Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype

Prenatal Diagnosis

Volumn 32, Issue 12, 2012, Pages 1166-1169

  Liao, Jun ^a,b   Sathanoori, Malini ^a,c   Yatsenko, Svetlana A ^a,c   Hu, Jie ^a,c   Kochmar, Sally J ^a   Hoffner, Lori ^c   Hogge, W Allen ^c   Surti, Urvashi ^a,b,c  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^c UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; ARTICLE; ARTIFACT; CHORION VILLUS SAMPLING; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME DELETION 22Q11; CHROMOSOME FRAGILE SITE; CHROMOSOME MOSAICISM; CYTOGENETICS; FEMALE; GESTATION PERIOD; HUMAN; HUMAN CELL; IN VITRO STUDY; MAJOR CLINICAL STUDY; MATERNAL BLOOD; PHENOTYPE; PREGNANCY OUTCOME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ULTRASOUND;

CELLS, CULTURED; CHORIONIC VILLI SAMPLING; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOME FRAGILE SITES; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; MOSAICISM; PHENOTYPE; PREGNANCY; PREGNANCY OUTCOME; PREGNANCY TRIMESTER, FIRST; PRENATAL DIAGNOSIS; PREVALENCE;

EID: 84870053861     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.3977     Document Type: Article

References (19)

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