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Bibliography

This is the list of the articles written on the syndromes of the chromosome 14.
Many of these are collected by our center. Those interested in receiving a copy may send a written request.


[2013] Epilepsy in ring 14 syndrome: A clinical and EEG study of 22 patients
Simona Giovannini, Lucia Marangio, Carlo Fusco, Angela Scarano, Daniele Frattini, Elvio Della Giustina, Marcella Zollino, Giovanni Neri and Giuseppe Gobbi
in Epilepsia

[2012] A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome.
Holder JL Jr, Lotze TE, Bacino C, Cheung SW.
in American Journal of Medical Genetics

[2012] Ring Chromosome 14 Mosaicism: An Unusual Case Associated With Developmental Delay and Epilepsy, Characterized by Genome Array-CGH
Anna Lisa Nucaro, Melania Falchi, Tiziana Pisano, Rossano Rossino, Francesca Boscarelli, Giusi Stoico, Angela Milia, Caterina Montaldo, Carlo Cianchetti, Dario Pruna
in American Journal of Medical Genetics

[2012] Linguistic and psychomotor development in children with chromosome 14 deletions
Laura Zampini, Laura D’odorico, Paola Zanchi, Marcella Zollino, & Giovanni Neri
in Clinical Linguistics & Phonetics

[2012] Epilepsy in ring 14 chromosome syndrome
Nicola Specchio, Marina Trivisano, Domenico Serino, Simona Cappelletti, Antonio Carotenuto, Dianela Claps, Carlo Efisio Marras, Lucia Fusco, Maurizio Elia, Federico Vigevano
in Epilepsy & Behavior

[2012] The ring 14 syndrome.
Zollino M, Ponzi E, Gobbi G, Neri G.
in Europenan Journal of Medical Genetics

[2011] The Proximal Chromosome 14q Microdeletion Syndrome: Delineation of the Phenotype Using High Resolution SNP Oligonucleotide Microarray Analysis (SOMA) and Review of the Literature
Edina Torgyekes, Alan L. Shanske, Kwame Anyane-Yeboa, Odelia Nahum, Sara Pirzadeh, Einat Blumfield, Vaidehi Jobanputra, Dorothy Warburton, and Brynn Levy
in American Journal of Medical Genetics

[2011] Competenze linguistiche in bambini di lingua italiana con aberrazioni del cromosoma 14
Laura D'Odorico, Simona Giovannini, Marinella Majorano, Laura Zampini,
in Scientific pubblication

[2010] Cytogenetic and Molecular Evaluation and 20-Year Follow-Up of a Patient With Ring Chromosome 14
Roberta Santos Guilherme, Vera de Freitas Ayres Meloni, Claudete Palmer Sodré, Denise Maria Christofolini, Renata Pellegrino, Claudia Berlim de Mello, Laura Kathleen Conlin, Anne Lawlor Hutchinson, Nancy Bettina Spinner, Decio Brunoni, Leslie Domenici Kul
in American Journal of Medical Genetics

[2010] Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome
Simona Giovannini, Daniele Frattini, Angela Scarano, Carlo Fusco, Gianna Bertani, Elvio Della Giustina, Paola Martinelli, Daniela Orteschi, Marcella Zollino, Giovanni Neri, Giuseppe Gobbi
in Epileptic Disord

[2010] A recurrent 14q32.2 microdeletion mediated by expanded TGG repeats
Frédérique Béna, Stefania Gimelli, Eugenia Migliavacca, Nathalie Brun-Druc, Karin Buiting, Stylianos E. Antonarakis and Andrew J. Sharp
in Human Molecular Genetics

[2009] Phenotypic Map in Ring 14 Syndrome
Marcella Zollino, Daniela Orteschi, and Giovanni Neri
in American Journal of Medical Genetics

[2009] The Ring14 Syndrome: Clinical and Molecular Definition
Zollino M., Seminara L., Orteschi D., Gobbi G., Giovannini S., Della Giustina E., Frattini D., Scarano A., Neri G.
in American Journal of Medical Genetics

[2009] Ring 14 chromosome presenting as early-onset isolated partial epilepsy
Dorothée Ville, Julitta De Bellescize, Marie Ange Nguyen, Hervé Testard, Agnès Gautier, Julie Perrier, Marianne Till, Vincent Des Portes
in Developmental Medicine & Child Neurology

[2009] 14q12 Microdeletion syndrome and congenital variant of Rett syndrome
Maria Antonietta Mencarelli, Tjitske Kleefstra, Eleni Katzaki, Filomena Tiziana Papa, Monika Cohen, Rolph Pfundt, Francesca Ariani, Ilaria Meloni, Francesca Mari, Alessandra Renieri
in Europenan Journal of Medical Genetics

[2009] Fenotipo elettro-clinico nella sindrome Ring14 e correlazioni col genotipo
d.ssa Giovannini
in Tesi di dottorato

[2007] Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion
Jeroen Knijnenburg, Arie van Haeringen, Kerstin BM Hansson, Arjan Lankester, Margot JM Smit, René DM Belfroid, Egbert Bakker, Carla Rosenberg, Hans J Tanke and Kàroly Szuhai
in Europenan Journal of Human Genetics

[2007] Supernumerary minute ring chromosome 14 in a man with primary infertility and left varicocele.
Stahl BC, Patil SR, Syrop CH, Sparks AE, Wald M
in Fertil Steril.

[2006] Deletion at 14q22-23 Indicates a Contiguous Gene Syndrome Comprising Anophthalmia, Pituitary Hypoplasia, and Ear Anomalies
Leisha D. Nolen, David Amor, Ashley Haywood, Luke St. Heaps, Chris Willcock, Marija Mihelec,Patrick Tam, Frank Billson, John Grigg, Greg Peters, and Robyn V. Jamieson
in American Journal of Medical Genetics

[2006] Is There a Higher Incidence of Maternal Uniparental Disomy 14 [upd(14)mat]? Detection of 10 New Patients by Methylation-Specific PCR
Diana Mitter, Karin Buiting, Ferdinand von Eggeling, Alma Kuechler, Thomas Liehr, Ulrike Angelika Mau-Holzmann, Eva-Christina Prott, Dagmar Wieczorek, and Gabriele Gillessen-Kaesbach
in American Journal of Medical Genetics

[2006] Terminal 14q32.33 Deletion: Genotype–Phenotype Correlation
M.-L. Maurin, S. Brisset, M. Le Lorc’h, V. Poncet, P. Trioche, A. Aboura, P. Labrune, G. Tachdjian
in American Journal of Medical Genetics

[2006] Ring Chromosome 14 with Epilepsy and Development Delay
Frenny J. Sheth, Nilang Soni.
in INDIAN PEDIATRICS

[2006] Molecular characterization of a novel translocation t(5;14)(q21;q32) in a patient with congenital abnormalities
Shawkat Haider,Rie Matsumoto Nobuyuki Kurosawa , Keiko Wakui Yoshimitsu Fukushima, Masaharu Isobe
in J Hum Genet

[2006] Ocular manifestations of chromosome 14 terminal deletion
Chung I, Chawla R, FitzGerald DE
in J Pediatr Ophthalmol Strabismus.

[2006] Prenatal diagnostic indicators of paternal uniparental disomy 14
Logos Curtis, Eric Antonelli, Yvan Vial, Peter Rimensberger, Martine Le Merrer, Christine Hinard, Armand Bottani, Siv Fokstuen
in PRENATAL DIAGNOSIS

[2005] A Paternally Derived Inverted Duplication of Distal 14q With a Terminal 14q Deletion
Chih-Ping Chen, Schu-Rern Chern, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Tzu-Hao Wang, Chen-Chi Lee,Chen-Wen Pan, Lie-Jiau Hsieh, and Wayseen Wang
in American Journal of Medical Genetics

[2005] A Paternally Derived Inverted Duplication of Distal 14q With a Terminal 14q Deletion
Chih-Ping Chen, Schu-Rern Chern, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Tzu-Hao Wang, Chen-Chi Lee, Chen-Wen Pan, Lie-Jiau Hsieh, and Wayseen Wang
in American Journal of Medical Genetics

[2005] FISH-Mapping of Telomeric 14q32 Deletions: Search for the Cause of Seizures
Kamilla Schlade-Bartusiak, Teresa Costa, Anne M. Summers, Malgorzata J.M. Nowaczyk, and Diane W. Cox
in American Journal of Medical Genetics

[2005] Maternal Uniparental Disomy 14 in a 15-Year-Old Boy With Normal Karyotype and No Evidence of Precocious Puberty
Stefan Aretz, Ruth Raff, Peter Propping, Joachim Woelfle, Marianne Esser. Klaus Zerres Thomas Eggermann
in American Journal of Medical Genetics

[2005] Molecular Characterization of a 14q Deletion in a Boy With Features of Holt–Oram Syndrome
Nathalie Le Meur,Alice Goldenberg, Christine Michel-Adde, Vale´rie Drouin-Garraud, Ge´rard Blaysat, Ste´phane Marret, Saad Abu Amara, He´le`ne Moirot, Ge´raldine Joly-He´las, Bertrand Mace, Pascale Kleinfinger,Pascale Saugier-Veber, Thierry Fre´bourg, A
in American Journal of Medical Genetics

[2005] Segmental and Full Paternal Isodisomy for Chromosome 14 in Three Patients: Narrowing the Critical Region and Implication for the Clinical Features
Masayo Kagami, Gen Nishimura, Torayuki Okuyama, Michiko Hayashidani, Toshio Takeuchi, Shinya Tanaka, Fumitoshi Ishino,Kenji Kurosawa, Tsutomu Ogata
in American Journal of Medical Genetics

[2005] Characterization of Chromosome 14 Abnormalities by Interphase In Situ Hybridization and Comparative Genomic Hybridization in 124 Meningiomas
María Dolores Tabernero, Ana Belén Espinosa, Angel Maíllo, José María Sayagués, María del Carmen Alguero, Eva Lumbreras, Pedro Díaz, Jesús María GonÇalves, Ignacio Onzain,Marta Merino, Francisco Morales, Alberto Orfao.
in Anatomic Pathology

[2005] Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture
Bregant L, Gersak K, Veble A
in Genet Couns.

[2005] Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes
Kamnasaran D, Chen CP, Devriendt K, Mehta L, Cox DW
in Genomics.

[2005] Haploinsufficiency of novel FOXG1Bvariants in a patient with severe mental retardation, brain malformations and microcephaly
Sarah A. Shoichet, Stella-Amrei Kunde , Petra Viertel Can Schell-Apacik , Hubertus von Voss Niels Tommerup , Hans-Hilger Ropers Vera M. Kalscheuer
in Hum Genet

[2004] Concerning ‘‘14q(22) Deletion in a Familial Case of Anophthalmia With Polydactyly’’
Gopalrao V.N. Velagaleti
in American Journal of Medical Genetics

[2004] Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis
Hou JW
in Chang Gung Med J.

[2004] Mosaic monosomy 14: clinical features and recognizable facies
V. McConnell, R. Derham, D. McManus and P.J. Morrison
in Clinical Dysmorphology

[2004] De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic features
Peippo M, Tengstrom C, Arvio M, Valanne L, Oksanen V, Kaakkola S, Ignatius J
in Genet Couns.

[2004] L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1
Meral Topc¸u, Florence Jobard, Sophie Halliez, Turgay Coskun, Cengiz Yalc¸inkayal, Filiz Ozbas Gerceker, Ronald J.A. Wanders, Jean-Franc¸ois Prud’homme, Mark Lathrop, Meral O¨ zguc3 and Judith Fischer
in Human Molecular Genetics,

[2004] Interstitial deletion of chromosome 14q in a Taiwanese infant with microcephaly
Su PH, Chen SJ, Lee IC, Wang KL, Chen JY, Hung HM, Lee CF.
in J Formos Med Assoc.

[2004] Loss of 14q chromosome in oligodendroglial and astrocytic tumors
Charles Dichamp, Sophie Taillibert, Lucinda Aguirre-Cruz, Julie Lejeune, Yannick Marie, Mich`ele Kujas, Jean-Yves Delattre, Khe Hoang-Xuan and Marc Sanson.
in Journal of Neuro-Oncology

[2004] Trisomy 14 Mosaicism: A Case Report and Review of the Literature
M. Fran Lynch, Caraciolo J. Fernandes, Lisa G. Shaffer, Lorraine Potocki.
in Journal of Perinatology

[2004] Ring chromosome 14 syndrome: a case report
Li R, Zhao ZY, Sun LY, Zheng X
in Zhonghua Er Ke Za Zhi.

[2003] 14q(22) Deletion in a Familial Case of Anophthalmia With Polydactyly (Clinical Report)
M.E. Ahmad, Rima Dada, Tanuj Dada, Kiran Kucheria
in American Journal of Medical Genetics

[2003] Stable Dicentric Duplication-Deficiency Chromosome 14 Resulting from Crossing-Over Within a Maternal Paracentric Inversion
Genevie`ve Lefort, Patricia Blanchet,Nabia Belgrade,Franc¸ois Rivier, Anne Marie Chaze, Pierre Sarda, Jacques Demaille, and Franck Pellestor.
in American Journal of Medical Genetics

[2003] Ring chromosome 14 with localization-related epilepsy: three cases
Masafumi Morimoto, Tomohiro Usuku, Masayuki Tanaka, Osamu Otabe, Akira Nishimura, Masaharu Ochi, †Yoshihiro Takeuchi, Hiroshi Yoshioka, and Tohru Sugimoto
in Epilepsia

[2003] A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3
R G Ruf, J Berkman, M T F Wolf, P Nurnberg, M Gattas, E-M Ruf, V Hyland, J Kromberg, I Glass, J Macmillan, E Otto, G Nurnberg, B Lucke, H C Hennies and F Hildebrandt
in J. Med. Genet.

[2003] Molecular characterisation of a 3.5 Mb 14q deletion in a child with several phenotypic anomalies
E Petek, B Plecko-Startinig, C Windpassinger, H Egger, K Wagner and P M Kroisel
in J. Med. Genet.

[2002] Further Delineation of the Chromosome 14q Terminal Deletion Syndrome
Clara D.M. van Karnebeek, Safira Quik, Sigrid Sluijter,Miriam M.F. Hulsbeek, Jan M.N. Hoovers, and Raoul C.M. Hennekam.
in American Journal of Medical Genetics

[2002] Subtelomeric FISH Uncovers Trisomy 14q32: Lessons for Imprinted Regions, Cryptic Rearrangements and Variant Acrocentric Short Arms
V. Reid Sutton, Karen J. Coveler, Seema R. Lalani, Catherine D. Kashork, Lisa G. Shaffer.
in American Journal of Medical Genetics

[2002] A case of segmental paternal isodisomy of chromosome 14
Karen J. Coveler · Sam P. Yang · V. Reid Sutton · Jay M. Milstein · Yuan-Qing Wu · Cami Knox-Du Bois · Linda S. Beischel · John P. Johnson · Lisa G. Shaffer
in Hum Genet

[2002] A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet.
Shinji Kondoh · Hirobumi Sugawara · Naoki Harada Naomichi Matsumoto · Hirofumi Ohashi · Masato Sato Piranit N. Kantaputra · Toshihiko Ogino · Hiroaki Tomita Tohru Ohta · Tatsuya Kishino · Yoshimitsu Fukushima Norio Niikawa · Koh-ichiro Yoshiura
in J Hum Genet

[2001] Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors.
Debiec-Rychter M, Sciot R, Pauwels P, Schoenmakers E, Dal Cin P, Hagemeijer A
in Genes Chromosomes Cancer.

[2000] Search for imprinted regions on chromosome 14:omparison on maternal and paternal UPD cases with cases of chromosome 14 deletions
V. Reid Sutton, Lisa G. Shaffer.
in American Journal of medical genetics

[2000] An adult patient with a distal interstitial 14q deletion: clinical report and literature review
Spruijt, Van Der Blij
in Genet Couns

[2000] 14q terminal deletion: prenatal diagnosis in a child with severe congenital anomalies
Mertens DJ, De Die-Smulders CE, Kampschoer PH, Offermans JP, Engelen JJ, Hamers AJ, Lammens M, Schrander-Stumpel CT
in Genet. Couns

[2000] 14: chromosomal mechanism and clinical follow up Maternal uniparental heterodisomy of chromosome
Munnich, M Vekemans and N Morichon-Delvallez D Sanlaville, M C Aubry, Y Dumez, M C Nolen, J Amiel, M P Pinson, S Lyonnet, A
in J. Med. Genet.

[2000] A case of ring 14 chromosome with ocular manifestation
Hisatomi, Kira
in Nippon Ganka Gakkai

[2000] A case of ring 14 chromosome with ocular manifestations
Hisatomi T, Kira R, Sakamoto T, Inomata H.
in Nippon Ganka Gakkai Zasshi.

[2000] Abnormal Myelination in a Patient With Deletion 14q11.2q13.1
Gian P. Ramelli, Karl O. Lo¨vblad, Hans Hirsiger, Hans Moser.
in PEDIATRIC NEUROLOGY

[1999] Ring chromosome 14 complicated with partial seizures and hypoplastic corpus callosum
Jiro Ono, Kazuhiko Nishiike, Katsumi Imai, Kazumasa Otani, and Shintaro Okada
in Pediatric Neurology

[1998] Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p
Meschede, Exeler
in Am J Med Genet

[1998] Ring chromosome 14: report of a new case
Campos, Casado
in An Esp Pediatr

[1997] Another case of maternal uniparental disomy chromosome 14 syndrome
Splitt, Goodship
in Am J Med Genet

[1997] Prenatal diagnosis of ring chromosome 14 after intracytoplasmic sperm injection
Jean, Rival
in Fertil Steril

[1997] Delineation of 14q32.3 deletion syndrome
A P Ortigas, Constance K Stein, Laura L Thomson, J J Hoo
in Journal of Medical Genetics

[1996] Good genes in bad neighbourhoods
Bedell, Jenkins
in Nat Genet

[1995] Molecular analysis redefines three human chromosome 14 deletion
Wintle, Costa
in Hum Genet

[1995] The detection of subtelometric chromosomal rearrangements in idiopatic mental retardation
Flint, Wilkie
in Nat Genet

[1994] A linkage map of human chromosome 14, including 13 gene loci
Cox, Billingsley
in Genomics

[1993] Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instabilty
Pezzolo, Gimelli
in Hum Genet

[1993] Epilepsy in a child with ring chromosome 14
Midro, Zadrozna
in Neurol Neurochir Pol

[1992] Childs with multgiple congenital anomalies and mosaicism 46,XX/46,Xxdel(14)(q32,2)
Miller, Jayakar
in Am J Med Genet

[1992] A further case of terminal (14)(q32.2) in a child with mild dysmorphic features
Wang, Allanson
in Ann Genet

[1992] Ring 14 chromosome with complex partial seizures: a case report
Shirasaka, Ito
in Brain Dev

[1992] Ring chromosome 14
Rudenskaia
in Pediatriia

[1992] The ring chromosome 14 syndrome
Kristensen, Wieg
in Ugeskr Laeger

[1991] Ring chromosome 14 Syndrome: report of two cases including extended evaluation of a previously reported patient and review
Zelante, Torricelli
in Ann Genet

[1991] Report of the commitee on the genetic constitution of chromosome 14
Cox, Nakamura
in Cytogenet Cell Genet

[1991] Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain gene: identification of a hot spot for recombination
Benger, Teshima
in Genomics

[1990] Pathogenesis of intracranial lipoma:an MR study in 42 patients
Truwit, Barkovich
in AJNR

[1990] Transmission of ring 14 chromosome from mother to two sons
Matalon, Supple
in Am J Med Genet

[1990] Syndrome r14 sans dysmorphie majeure
Blois, Caille
in Ann Genet

[1990] Physical mapping of probes within 14q32, a subteloremic region showing high recombination frequency
Hofker, Smith
in Genomics

[1990] Terminal deletion (14)(q32.3): a new case
Telford, Thomson
in Med Genet

[1989] Epilepsy in ring chromosome 14 syndrome
Duarte, Lison
in Arq Neuropsiquiatr

[1989] Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation
Cantù, Thomas
in Clin Genet

[1989] Molecular characterization of a ring chromosome 14 showing that the PI locus is Centrometric to the D14S1 and IGH loci
Keyeux, Gilgenkrantz
in Hum Genet

[1989] A terminal deletion (14) (q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation
Yen, Podruch
in J Med Genet

[1988] Retinal/macular pigmentation in conjunction with ring 14 chromosome
Howard, Clark
in Hum Genet

[1987] Ring chromosome 14 without deletion
Angelova, Mitreva
in Acta Pediatr Hung

[1987] A primary genetic linkage map of distal chromosome 14q
Nakamura, Leppert
in Cytogent Cell Genet

[1987] Does ring syndrome exist? An analysis of 207 case reports on patients with a ring autosome
Kosztolanyi
in Hum Genet

[1986] Clinical findings in an arab boy with ring (14)(mos 46,XY,r(14)/45,XY,-14)
Portoian-Shuhaiber
in Ann Genet

[1986] Ocular findings in a patient with deletion short arm chromosome 5 (cri-du-chat) and ring 14 chromosome
Clark, Howard
in Trans Ophthalmol Soc UK

[1985] 2 new cases of ring chromosome 14
Caille, Rethore
in Ann Pediatr

[1985] Distal monosomy 14 not associated with ring formation
Hreidarsson, Stamberg
in J Med Genet

[1984] Ring chromosome 14 and immunoglobulin locus
Krawczun, Melink
in Am J Med Genet

[1984] Chromosome 14 en anneau une observation de r(14) en mosaique le phènotype r(14)
Rethoré, Caille
in Ann Genet

[1984] Chromosome 14 en anneau une observation de r(14) homogène
Raolu, Razavi
in Ann Genet

[1984] Ring-14 and trisomyq in the same child
Pangalos, Velissariou
in Ann Genet

[1984] The r(14) syndrome. Three new observations
Gilgenkrantz, Morali
in Ann Genet

[1983] Anomalies oculaires du phénotype 46,XY,r(14)
Guillot, Dufier
in Arch Fr Pediatr

[1983] Ring 14 syndrome with decreased bone mineral content in two pubertal Girls
Ieshima, Takeshita
in Hum Genet

[1983] Ring chromosome 14. A distinct clinical entity
Fryns, Kubien
in J Genet Hum

[1983] Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus
Linsley, Bech-Hansen
in Proc Natl Acad Sci USA

[1982] Ring chromosome 14 syndrome
Fryns, Petit
in Ann Genet

[1981] Ring 14 chromosome: association with seizures
Lippe, Sparkes
in Am J Med Genet

[1981] Infant male with ring chromosome 14
Triolo, Serra
in Ann Genet

[1981] Ring 15 chromosome
Yunis, Leibovici
in Hum Genet

[1981] Inheritance of a ring 14 chromosome
S Bowser Riley, K E Buckton, S G Ratcliffe, and J Syme
in J Med Genet

[1981] Ring chromosome 14: a distinct clinical entity
Rina Schmidt, Lydia Eviatar, Harold M Nitowsky, Martha Wong, and Sylvia Miranda
in J Med Genet

[1980] Ring chromosome 14 in a mentally retarded girl
Iselius, Ritzen
in Acta Pediatr Scand

[1980] A Ring 14 chromosome with deleted short arm
Amarose, Huttenlocher
in Hum Genet

[1980] Ring 14 chromosome and choreoathetosis
McBride, Oppenheimer
in Neurology

[1979] Ring chromosome 14 identified by banding thecniques
Vekemans, Watters
in Am J Med Genet

[1979] Ring chromosome 22 in a mentally retarded child and mosaic 45,XX - 15 - 22,t(15:22)(p11q11)/46XXr(22)/46,XX karyotipe in the mother
Fryns, Van Der Berghe
in Hum Genet

[1979] Chromosomal location of the genes for human immunoglobulin heavy chains
Croce, Shander
in Proc Natl Acad Sci USA

[1978] Formation of a ring chromosome 14 subsequent to the de novo 13/14 reciprocal translocation: a new cytogenetic evidence obtained by nucleolus-organizer staining
Abe, Misawa
in Ann Genet

[1978] Cromosoma 14 ad anello
Torricelli, Giovannucci
in Nuove sindromi cromosomiche patologia autosomica soc Ed Universo

[1977] Extended evaluation of previously reported twins with a ring 14 chromosome
Sparkes, Klisak
in Ann Genet

[1977] Ring chromosome 14 in monozygotic twins
Jalbert, Sele
in Ann Genet

[1977] Four new cases of ring 21 and 22 including familial transmission of ring 21
Palmer, Hodes
in J Med Genet

[1977] Multiple congenital malformations in a child with ring 14 chromosome
Dzarlieva
in Med Fak Skopje

[1976] The adolescent growth spurt of boys and girls of the Harpenden Growth study
Tanner, Whitehouse
in Ann Hum Biol

[1975] Differential staining of the satellite regions of Human chromosomes
Howell, Denton
in experientia

[1974] The behavior of ring chromosome 13
Hoo, Obermann
in Humanagenetik

[1973] A familial case of 17R ring shaped chromosome of group E with transmission from father to son
Burden, Lupascu
in Rev Med Chir Soc Med Nat Iasi

[1971] Le syndrome Dr. Etude d'un nouveau cas
Gilgenkrantz, Cabrol
in Ann Genet

[1971] Meiotic studies in a subfertile patient with a ring chromosome
Chandley, Edmond
in Cytogenetics

[1971] Ring chromosome 18 in mother and daughter
Christensen, Friedrich
in J Ment Defic Res

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