SCOPUS 정보 검색 플랫폼

Lancet

Volumn 354, Issue 9191, 1999, Pages 1659-1660

Defining the chromosomal basis of mental handicap

(2) Hamerton, J L a Stranc, L a

a UNIVERSITY OF MANITOBA (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CHROMOSOME TRANSLOCATION; CYTOGENETICS; DIAGNOSTIC ACCURACY; DISEASE SEVERITY; DNA PROBE; FAMILIAL DISEASE; GENETIC SCREENING; HUMAN; HUMAN CELL; KARYOTYPE; MENTAL DEFICIENCY; NOTE; PHENOTYPE; PRIORITY JOURNAL; TELOMERE;

EID: 0033552496 PISSN: 01406736 EISSN: None Source Type: Journal
DOI: 10.1016/S0140-6736(99)00246-9 Document Type: Note

Times cited : (3)

References (8)

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2
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3
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- Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms.
- K Brondum-Nielsen B Beck J Gyftodimou Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms. Hum Genet 99 1997 56 61
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- Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11.
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5
- 0027331380
- Miller-Dieker syndrome: detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring.
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6
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- Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father.
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7
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- Deletion of 22q11 in two brothers with different phenotype.
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8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.