9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism

Author:

Quinonez Shane C.1,Park John M.2,Rabah Raja3,Owens Kailey M.1,Yashar Beverly M.4,Glover Thomas W.,Keegan Catherine E.

Affiliation:

1. Department of Pediatrics, Division of Genetics; University of Michigan; Ann Arbor; Michigan

2. Department of Urology; University of Michigan; Ann Arbor; Michigan

3. Department of Pathology; University of Michigan; Ann Arbor; Michigan

4. Department of Human Genetics; University of Michigan; Ann Arbor; Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference111 articles.

1. A severely mental and motor retarded boy with monosomy 9pter->p22 trisomy 10q26->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26);Akbas;Genet Couns,2011

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

3. The 9p- syndrome;Alfi;Ann Génét,1976

4. A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardation;Argyriou;Clin Dysmorphol,2010

5. De novo duplication of 7pter->p21.2 and deletion of 9pter->p23.5: Clinical and cytogenetic diagnosis;Back;Clin Genet,1997

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