Prenatal Detection of Cryptic Genomic Rearrangement: Role of Detailed Family History, Pedigree Analysis and Advanced Genomic Technologies

Author:

Sheth Frenny J

Publisher

MedCrave Group, LLC

Reference13 articles.

1. Snijders R, Nicolaides KH. Ultrasound markers for fetal chromosome defects. In: Nicolaides KH, editors. Frontiers in Fetal Medicine Series. London, UK; 1996. p. 21‒55.

2. Reproductive risks for translocation carriers: cytogenetic study and analysis of pregnancy outcome in 58 families;Neri;Am J Med Genet,1983

3. Sachs ES, Jahoda MG, Van Hemel JO, et al. Chromosome studies of 500 couples with two or more abortions. Obstet Gynecol. 1985;65(3):375‒378.

4. First-trimester prenatal diagnosis of a familial subtelomeric translocation;Kilby;Ultrasound Obstet Gynecol,2001

5. 3 monosomy: definition of minimum deletion intervals for key phenotypes;Aldred;J Med Genet,2004

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