SCOPUS 정보 검색 플랫폼

Volumn 38, Issue 3, 2001, Pages 175-178

Submicroscopic subtelomeric 1qter deletions: A recognisable phenotype? [1]

(6) De Vries, B B A a Knight, S J L a Homfray, T a Smithson, S F a Flint, J a Winter, R M a

a UNIVERSITY COLLEGE LONDON (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CHROMOSOME 1Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; DISEASE COURSE; FEMALE; FETUS; HUMAN; IN SITU HYBRIDIZATION; KARYOTYPE 46,XY; LETTER; MALE; MENTAL DEFICIENCY; PHENOTYPE; PRIORITY JOURNAL; TELOMERE; TRISOMY 13;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; FAMILY HEALTH; FATAL OUTCOME; FEMALE; FETUS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; PHENOTYPE; TELOMERE;

EID: 0035083965 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (62)

References (12)

1
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2
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10
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11
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12
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.