Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q
Author:
Funder
PROMEP
PAICYT
CONACYT
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference26 articles.
1. The critical region on the human Xq;Therman;Hum Genet,1990
2. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992
3. The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes;Young;Hum Genet,1982
4. Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique;Keitges;Hum Genet,1986
5. Hypoplastic external genitalia in association with X;autosome chromosome translocation;Omar;J Pediatr Adolesc Gynecol,1999
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