46,XY,18q+/46,XY,18q− mosaicism in a fragile X prenatal diagnosis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference15 articles.
1. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.
2. 1990Birth Defects Encyclopedia. The Center for Birth Defects Information Services, IncBlackwell Scientific Publications: Dover, MA; 385-388
3. Prenatal diagnosis of fragile x syndrome: (cgg)n expansion and methylation of chorionic villus samples
4. PRENATAL DIAGNOSIS OF A DELETION OF 18q IN A FETUS ASSOCIATED WITH MULTIPLE-MARKER SCREEN POSITIVE RESULTS
5. Prenatal diagnosis of de novo mosaic distal 18q deletion associated with congenital anomalies
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1. Mosaicos cromosómicos en vellosidad corial;Diagnóstico Prenatal;2013-07
2. Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses;Reproductive BioMedicine Online;2010-10
3. Duplication/deletion mosaicism of the 7q(21.1 → 31.3) region;American Journal of Medical Genetics Part A;2007-01-15
4. Current awareness in prenatal diagnosis;Prenatal Diagnosis;2005
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