Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin

Prenatal Diagnosis

Volumn 16, Issue 11, 1996, Pages 1021-1026

  Paulyson, Kristin J ^a,c   Sherer, David M ^a   Christian, Susan L ^b   Lewis, Kerry M ^a   Ledbetter, David H ^b   Salafia, Carolyn M ^a   Meck, Jeanne M ^a  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Amniocentesis; Mosaic trisomy 16; Paternal non disjunction; Prenatal diagnosis; Prenatal ultrasound

Indexed keywords

ALPHA FETOPROTEIN;

ADULT; AMNIOCENTESIS; AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; CYTOGENETICS; FACE DYSMORPHIA; FEMALE; FETUS; FETUS DISTRESS; FETUS MONITORING; FETUS MOVEMENT; HUMAN; INTRAUTERINE GROWTH RETARDATION; MOSAICISM; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SKIN FIBROBLAST; TRISOMY;

ALPHA-FETOPROTEINS; AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 16; CRANIOFACIAL ABNORMALITIES; FATHERS; FEMALE; FETAL DISTRESS; FETAL GROWTH RETARDATION; GESTATIONAL AGE; HEART DEFECTS, CONGENITAL; HUMANS; MOSAICISM; PLACENTA; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

EID: 0029848641     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199611)16:11<1021::AID-PD963>3.0.CO;2-I     Document Type: Article

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