De novo trisomy 16p11.2-qter: Report of an infant

American Journal of Medical Genetics

Volumn 92, Issue 5, 2000, Pages 308-310

  Masuno, Mitsuo ^a   Ishii, Takuma ^a,b   Tanaka, Yukichi ^a   Ohyama, Makiko ^a   Kawataki, Motoyoshi ^a   Kimura, Junko ^a   Imaizumi, Kiyoshi ^a   Kuroki, Yoshikazu ^a  

^a KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

^b ASAHIKAWA MEDICAL COLLEGE   (Japan)

Author keywords

Maternal meiosis; Nondisjunction; Short tandem repeat typing; Trisomy 16q

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 16P; CLINICAL FEATURE; CYTOGENETICS; FEMALE; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; PRIORITY JOURNAL; SYNDROME DELINEATION; TANDEM REPEAT; TRISOMY;

CHROMOSOMES, HUMAN, PAIR 16; FEMALE; HUMANS; INFANT, NEWBORN; KARYOTYPING; TRISOMY;

EID: 0034686414     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20000619)92:5<308::AID-AJMG3>3.0.CO;2-6     Document Type: Article

References (7)

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