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Volumn 2001, Issue 1, 2001, Pages 45-47

The impact of genetic diseases on Jordanians: Strategies towards prevention

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; BETA THALASSEMIA; CONSANGUINEOUS MARRIAGE; CYSTIC FIBROSIS; DNA POLYMORPHISM; FAMILIAL MEDITERRANEAN FEVER; GENETIC COUNSELING; GENETIC DISORDER; GENETIC SCREENING; HETEROZYGOTE DETECTION; HUMAN; INBREEDING; INFANT MORTALITY; JORDAN; LETTER; MEDICAL EXAMINATION; NEWBORN SCREENING; POPULATION GENETICS; PRENATAL SCREENING; PUBLIC HEALTH SERVICE; RURAL POPULATION; URBAN POPULATION;

EID: 34249679670     PISSN: 11107243     EISSN: 11107251     Source Type: Journal    
DOI: 10.1155/S1110724301000092     Document Type: Letter
Times cited : (13)

References (11)
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  • 2
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  • 3
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    • Teebi, A.S.1
  • 4
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    • Progressive pseudorheumatoid dysplasia: Report of a family and review
    • El-Shanti H, Omari HZ, Qubain HI. Progressive pseudorheumatoid dysplasia: Report of a family and review. J Med Genet. 1997;34:559-563.
    • (1997) J Med Genet , vol.34 , pp. 559-563
    • El-Shanti, H.1    Omari, H.Z.2    Qubain, H.I.3
  • 5
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    • Normative standards of trunk and limb anthropometric measurements for Jordanian newborns
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    • El-Shanti, H.1    Al-Lahham, M.B.2    Batieha, A.3
  • 7
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    • A clinical study of a large inbred kindred with pure familial spastic paraplegia
    • El-Shanti H, Daoud AS, Batieha A. A clinical study of a large inbred kindred with pure familial spastic paraplegia. Brain Dev. 1999;21:478-482.
    • (1999) Brain Dev , vol.21 , pp. 478-482
    • El-Shanti, H.1    Daoud, A.S.2    Batieha, A.3
  • 8
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    • The assignment of the gene responsible for progressive pseudorheumatoid Dysplasia to chromosome six and examination of COL10A1 as a candidate gene
    • El-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, Al-Alami J. The assignment of the gene responsible for progressive pseudorheumatoid Dysplasia to chromosome six and examination of COL10A1 as a candidate gene. Eur J Hum Genet. 1998;6:251-256.
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    • El-Shanti, H.1    Murray, J.C.2    Semina, E.V.3    Beutow, K.H.4    Scherpbier, T.5    Al-Alami, J.6
  • 9
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    • Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia
    • Hurvitz JR, Suwairi WM, Van Hul W, et al. Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia. Nat Genet. 1999;23:94-98.
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  • 10
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    • Fine mapping of progressive pseudorheumatoid dysplasia: A tool for heterozygote identification
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    • A nonsense mutation in the retinal-specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred kindred from Jordan
    • El-Shanti H, Al-Salem M, El-Najjar M, et al. A nonsense mutation in the retinal-specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred kindred from Jordan. J Med Genet. 1999;36:862-865.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.