Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy

Author:

Chen Chih-Ping,Su Yi-Ning,Hsu Chin-Yuan,Chern Schu-Rern,Lee Chen-Chi,Chen Yu-Ting,Chen Wen-Lin,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference45 articles.

1. Familial de Lange syndrome with chromosome abnormalities;Falek;Pediatrics.,1966

2. Aneusomies de recombinaision. Conséquence d’une inversion pericentrique d’un chromosome 3 paternel;Boué;Ann Pediatr.,1974

3. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21);Allderdice;Am J Hum Genet.,1975

4. Duplication-deletion of chromosome 3 syndrome;Patil;Am J Hum Genet.,1978

5. A case of chromosome 3 duplication q deletion p syndrome born to the mother with a pericentric inversion, inv(3)(p25q21);Kawashima;Jinrui Idengaku Zasshi.,1979

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