Ring 20 chromosome phenotype.

Author:

Porfirio B,Valorani M G,Giannotti A,Sabetta G,Dallapiccola B

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. Useftulness of chromosome catalog in delincating new svndromes;l Borgaonkar DS; C, Lacassic Y.E.Stoll;Birtli Defects,1976

2. A ring-29) chromosomc;M, Atkins L.Miller W.L.Salam;J Med Getnet,1972

3. Ring F chromosome mosaicism (46. XY.20r/46. XY) in an cpileptic child without apparent haematological disease;HG, Faed M.Morton; J, Robertson;J Med Geniet,1972

4. Ring formation of chromosomes Nos 19 and 20;CC, Uchida I.A.Lin,1972

5. Ring 2(0 chromosome in a child with seizures. minor anomalies, and retardation;DT, Stewart J.M.Cavanagh N.Hughes;Arcli Dis Child; 54: 477-9. " Herva R. Saarinen I. Lcikkonen L. The r(20) syndrome,1979

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1. Case Report: A Paternal 20q13.2-q13.32 Deletion Patient With Growth Retardation Improved by Growth Hormone;Frontiers in Genetics;2022-03-24

2. R;Synopsis of Neurology, Psychiatry and Related Systemic Disorders;2019-05-23

3. Specificity of electroclinical features in the diagnosis of ring chromosome 20;Epilepsy & Behavior;2018-03

4. First Report of Low-Rate Mosaicism for 20q11.21q12 Deletion and Delineation of the Associated Disorder;Cytogenetic and Genome Research;2018

5. Ring Chromosome 20 Syndrome and Epilepsy;Journal of Pediatric Epilepsy;2015-07-03

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