Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH

American Journal of Medical Genetics, Part A

Volumn 146, Issue 6, 2008, Pages 764-769

  Wood, Elizabeth ^a,c   Dowey, Sarah ^a   Saul, Daniel ^a   Cain, Colyn ^a   Rossiter, Judith ^a,b   Blakemore, Karin ^a   Stetten, Gail ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Perinatal Center   (United States)

^c JOHNS HOPKINS HOSPITAL   (United States)

Author keywords

Array CGH; Mosaicism; Trisomy 8q

Indexed keywords

AMNIOCENTESIS; ANEUPLOIDY; ARTICLE; CASE REPORT; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME MOSAICISM; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FETUS; FETUS ECHOGRAPHY; FETUS MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; HUMAN; KARYOTYPE; MOSAIC TRISOMY 8Q; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SECOND TRIMESTER PREGNANCY; TRISOMY 8; WARKANY SYNDROME;

ADULT; AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 8; CYTOGENETIC ANALYSIS; FEMALE; HUMANS; MOSAICISM; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PREGNANCY; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

EID: 40449118234     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32184     Document Type: Article

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