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American Journal of Medical Genetics

Volumn 95, Issue 5, 2000, Pages 411-414

Possible isochromosome 22 leading to trisomy 22

(4) Manasse, Bridget F a Pfaffenzeller, Wilma M a Gurtunca, Nursen b De Ravel, Thomy J L a,c

a UNIVERSITY OF THE WITWATERSRAND (South Africa)

b UNIVERSITY OF THE WITWATERSRAND (South Africa)

c NATIONAL HEALTH LABORATORY SERVICE (South Africa)

Author keywords

Isochromosome 22; Monocentric; Trisomy 22

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 22; FACE MALFORMATION; FEMALE; GENITAL MALFORMATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; INFANT; ISOCHROMOSOME; LIFESPAN; PRIORITY JOURNAL; SURVIVAL; TRISOMY;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 22; FACE; FEMALE; GENITALIA, FEMALE; GROWTH DISORDERS; HEART SEPTAL DEFECTS, ATRIAL; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT, NEWBORN; ISOCHROMOSOMES; KARYOTYPING; MALE; MONOSOMY; PHENOTYPE; PREGNANCY; PREGNANCY COMPLICATIONS; TRISOMY;

EID: 0034684720 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(20001218)95:5<411::AID-AJMG1>3.0.CO;2-Q Document Type: Article

Times cited : (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.