Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies

Author:

Hou Wen-Chien,Chen Chih-Ping,Hwang Kwei-Shuai,Chen Ying-Chieh,Lai Yu-Ju,Tien Chau-Yang,Su Her-Young

Funder

Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference30 articles.

1. Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23;Kawara;Am J Med Genet A,2006

2. Short clinical report: a new case with de novo partial 9p monosomy;Nagy;Acta Paediatr Hung,1991

3. The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation;Orye;Clin Genet,1975

4. Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations;Sirisena;Case Rep Genet,2013

5. Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype;Swinkels;Am J Med Genet A,2008

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