Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: Chromosomal distribution, clinical findings, and UPD studies

European Journal of Human Genetics

Volumn 13, Issue 11, 2005, Pages 1192-1204

  Bartsch, Oliver ^a,b   Loitzsch, Anne ^b   Kozlowski, Peter ^c   Mazauric, Marie Luise ^c   Hickmann, Gabriele ^c  

^a UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^c Prenatal Diagnosis and Genetics   (Germany)

Author keywords

Clinical outcome; Frequency; Prenatal diagnosis; Supernumerary marker chromosomes; Uniparental disomy

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 22Q; CLINICAL ARTICLE; EUCHROMATIN; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HUMAN; KIDNEY DYSPLASIA; PALLISTER KILLIAN SYNDROME; PREGNANCY; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PREVALENCE; PRIORITY JOURNAL; SPINA BIFIDA; SUPERNUMERARY CHROMOSOME; UNIPARENTAL DISOMY; AMNIOCENTESIS; ANEUPLOIDY; CASE REPORT; CHILD; CHORION VILLUS SAMPLING; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CLASSIFICATION; FETUS; GENETIC MARKER; GENETIC SCREENING; GENETICS; HEALTH SURVEY; INFANT; KARYOTYPING; MALE; MULTIPLE MALFORMATION SYNDROME; PRESCHOOL CHILD; STATISTICS;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AMNIOCENTESIS; ANEUPLOIDY; CHILD; CHILD, PRESCHOOL; CHORIONIC VILLI SAMPLING; CHROMOSOME ABERRATIONS; CYTOGENETIC ANALYSIS; FEMALE; FETUS; GENETIC MARKERS; GENETIC SCREENING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; POPULATION SURVEILLANCE; PREGNANCY; PRENATAL DIAGNOSIS; UNIPARENTAL DISOMY;

EID: 33644812402     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201473     Document Type: Article

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