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Volumn 332, Issue 8618, 1988, Pages 1005-1007

GENETICS OF CLASSIC ALPORT'S SYNDROME

Author keywords

[No Author keywords available]

Indexed keywords

ALPORT SYNDROME; FAMILY; GENETIC LINKAGE; HEREDITY; HUMAN; NEPHRITIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; X CHROMOSOME ABERRATION;

EID: 0023775025     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(88)90753-2     Document Type: Article
Times cited : (182)

References (49)
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  • 9
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  • 10
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  • 15
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    • A heredo-familial syndrome characterised by renal disease, inner ear deafness and ocular changes
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  • 18
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    • Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?
    • (1983) Br J Ophthalmol , vol.67 , pp. 493-503
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  • 19
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  • 24
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    • Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies
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    • 84919592930 scopus 로고    scopus 로고
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  • 32
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    • Further scoring types in sequential linkage tests with a critical review of autosomal and partial sex linkage in man
    • (1957) Am J Hum Genet , vol.9 , pp. 55-75
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  • 33
    • 70449312366 scopus 로고
    • Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred
    • (1959) Am J Hum Genet , vol.11 , pp. 333-338
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    • (1961) Am J Hum Genet , vol.13 , pp. 89-97
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.