t(15;21)(q15;q22.1)pat Resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring

American Journal of Medical Genetics

Volumn 66, Issue 1, 1996, Pages 45-51

  Abeliovich, Dvorah ^a   Dagan, Judith ^a   Lerer, Israela ^a   Silberstein, Shira ^a   Katznelson, Mariassa Bat Miriam ^b   Frydman, Moshe ^c  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b SHEBA MEDICAL CENTER   (Israel)

^c HASHARON HOSPITAL   (Israel)

Author keywords

D21S213; D21S217; duplication 15(pter > q15); partial monosomy 21; partial trisomy 21; Prader Willi syndrome; translocation breakpoint

Indexed keywords

DNA;

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 15; CHROMOSOME 21; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; DERMATOGLYPHICS; DNA METHYLATION; FEMALE; GENE; HUMAN; HUMAN CELL; MALE; PARTIAL MONOSOMY; PARTIAL TRISOMY; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PROGENY; SIBLING; SOUTHERN BLOTTING;

ADOLESCENT; CHILD; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 21; FEMALE; GENETIC MARKERS; HUMANS; KARYOTYPING; MALE; MONOSOMY; PEDIGREE; SYNDROME; TRANSLOCATION, GENETIC; TRISOMY;

RAPHIA FRATER;

EID: 0029857915     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961202)66:1<45::AID-AJMG10>3.0.CO;2-Q     Document Type: Article

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