A live-born child with a mosaic chromosomal pattern of either monosomy 21 or trisomy 4 in different embryonal germ layers

Prenatal Diagnosis

Volumn 30, Issue 1, 2010, Pages 86-88

  Van Der Kevie Kersemaekers, A M F ^a   Suijkerbuijk, R F ^a   Moll, F C P ^b   Dijkhuizen, T ^a   Van Spaendonck Zwarts, K Y ^a   Drok, G ^a   Bouman, K ^a   Sikkema Raddatz, B ^a  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b ISALA HOSPITAL   (Netherlands)

Author keywords

Embryonal germ layers; Monosomy 21; Mosaicism; Prenatal; Trisomy 4

Indexed keywords

DNA;

ADULT; AMNIOCENTESIS; AMNION CELL; ARTICLE; AUTOPSY; CASE REPORT; CHROMOSOME ANALYSIS; CONGENITAL MALFORMATION; CYTOGENETICS; DNA DETERMINATION; DNA ISOLATION; EMBRYO CELL; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GERM LAYER; GESTATIONAL AGE; HUMAN; HUMAN TISSUE; MALE; METAPHASE; MONOSOMY 21; MOSAICISM; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NEWBORN; PRIORITY JOURNAL; TRISOMY 4;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 4; FATAL OUTCOME; FEMALE; GERM LAYERS; HUMANS; INFANT, NEWBORN; MALE; MONOSOMY; MOSAICISM; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 75149168559     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2415     Document Type: Article

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