Am J Med Genet. 2000 Dec 11;95(4):316-9.

Partial trisomy 20p: familial occurrence.

Oppenheimer S, Dignan P, Soukup S.

Source

Cincinnati Center Developmental Disabilities, Cincinnati Children's Hospital, Ohio 45229, USA.

Abstract

Partial trisomy 20p syndrome in an uncle and niece are compared to 32 previous cases.

PMID:: 11186883; [PubMed - indexed for MEDLINE]

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Cited by 2 PubMed Central articles

A case of partial trisomy 20p resulting from meiotic recombination of a maternal pericentric inversion. [Ann Lab Med. 2012]
A case of partial trisomy 20p resulting from meiotic recombination of a maternal pericentric inversion.
Kang JE, Park MY, Cheon CK, Lee HD, Hwang SH, Yi J. Ann Lab Med. 2012 Jan; 32(1):91-4. Epub 2011 Dec 20.
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. [Am J Med Genet A. 2011]
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.
Freitas ÉL, Gribble SM, Simioni M, Vieira TP, Silva-Grecco RL, Balarin MA, Prigmore E, Krepischi-Santos AC, Rosenberg C, Szuhai K, et al. Am J Med Genet A. 2011 Nov; 155A(11):2754-61. Epub 2011 Sep 21.

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