A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review-Reference-Cited by-同舟云学术

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A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review

Published:2006-09 Issue:5 Volume:49 Page:402-413
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Courtens Winnie,Wuyts Wim,Scheers Stefaan,Van Luijk Rob,Reyniers Edwin,Rooms Liesbeth,Ceulemans Berten,Kooy Frank,Wauters Jan

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference34 articles.

1. A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region;Bartsch;Hum. Genet.,1997

2. Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH);Benzacken;Clin. Genet.,1998

3. Pure trisomy 10p involving an isochromosome 10p;Berend;Clin. Genet.,1999

4. Trisomy 10p: report of an unusual mechanism of formation and critical evaluation of the clinical phenotype;Clement;Am. J. Med. Genet.,1996

5. Preferential loss of the paternal alleles in the 18q- syndrome;Cody;Am. J. Med. Genet.,1997

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature;Cureus;2021-07-26

2. Jacobsen syndrome and neonatal bleeding: report on two unrelated patients;Italian Journal of Pediatrics;2021-07-01

3. A Rare and Unusual Case of Trisomy 10p with Terminal 14q Deletion: A Multidisciplinary Approach;Cureus;2021-06-05

4. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients;American Journal of Medical Genetics Part A;2012-03-09

5. Detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation;Orvosi Hetilap;2010-07-01

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