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Volumn 61, Issue 5, 1997, Pages 1139-1143

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter

Author keywords

[No Author keywords available]

Indexed keywords

ARAB; ARTHROGRYPOSIS; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 5Q; CLINICAL ARTICLE; FEMALE; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; INBREEDING; ISRAEL; JOINT CONTRACTURE; MALE; NEUROPATHY; PEDIGREE; PRIORITY JOURNAL;

EID: 0030731114     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301598     Document Type: Article
Times cited : (20)

References (18)
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  • 2
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  • 4
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    • Cerebral lesions in arthrogryposis multiplex congenita
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    • Ek, J.I.1
  • 6
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    • Arthrogryposes (multiple congenital contractures)
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    • Hall JH (1996) Arthrogryposes (multiple congenital contractures). In: Emery AE, Rimoin DL (eds) Principles and practice of medical genetics, 3d ed. Churchill Livingstone, New York, pp 2869-2916
    • (1996) Principles and Practice of Medical Genetics, 3d Ed. , pp. 2869-2916
    • Hall, J.H.1
  • 8
    • 0026657630 scopus 로고
    • Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community
    • Jaber L, Merlob P, Bu X, Rotter JI, Shohat M (1992) Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community. Am J Med Genet 44:1-6
    • (1992) Am J Med Genet , vol.44 , pp. 1-6
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  • 10
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    • 0023239442 scopus 로고
    • Homozygosity mapping: A way to many human recessive traits with the DNA of inbred children
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  • 15
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  • 17
    • 16944364790 scopus 로고
    • Multiple congenital contractures (arthrogryposis): Nature of the syndrome and hereditary considerations
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.