Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry

Author:

Chen Chih-Ping,Su Yi-Ning,Lin Shuan-Pei,Chern Schu-Rern,Su Jun-Wei,Chen Yu-Ting,Lee Meng-Shan,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference18 articles.

1. Duplication 11 (q21 to 23 leads to qter) syndrome;Francke;Birth Defects Orig Artic Ser,1977

2. Upper airway malformation associated with partial trisomy 11q;Zhao;Am J Med Genet A,2003

3. ‘Pure’ partial trisomy 11q (11q23.1→11qter): expanding the phenotype;Zimberg-Bossira;Clin Dysmorphol,2011

4. Duplication and deletion 11q23-q24 recombinants in two offspring of an intrachromosomal insertion (“shift”) carrier;Forsythe;Henry Ford Hosp Med J,1988

5. Tandem duplication 11q23-ter in the dysmorphic child of a retarded mother mosaic for the same anomaly with no apparent abnormalities;Pfeiffer;Ann Genet,1993

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