Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization

Author:

Freitas Érika L.,Gribble Susan M.,Simioni Milena,Vieira Társis P.,Silva-Grecco Roseane L.,Balarin Marly A. S.,Prigmore Elena,Krepischi-Santos Ana C.,Rosenberg Carla,Szuhai Karoly,van Haeringen Arie,Carter Nigel P.,Gil-da-Silva-Lopes Vera Lúcia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference40 articles.

1. Deletion of the short arm of chromosome #9 (46,9p-): A new deletion syndrome;Alfi;Ann Genet,1973

2. Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency;Araújo;Braz J Med Biol Res,1996

3. Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA;Barbaro;Eur J Hum Genet,2009

4. A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal;Bardoni;Nat Genet,1994

5. Deletion 9p and sex reversal;Bennett;J Med Genet,1993

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