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Volumn 45, Issue 2, 2004, Pages 108-110

Early diagnosis of Prader-Willi syndrome in a newborn

Author keywords

Hypotonia; Newborn; Prader Willi syndrome

Indexed keywords

SMALL NUCLEAR RIBONUCLEOPROTEIN; SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE N; UNCLASSIFIED DRUG;

EID: 3142683602     PISSN: 16088115     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (12)
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  • 2
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  • 3
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    • (1995) Neurology of the Newborn, 3rd Ed. , pp. 606-633
    • Volpe, J.J.1
  • 5
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    • The neonatal presentation of Prader-Willi syndrome revisited
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    • Miller, S.P.1    Riley, P.2    Shevell, M.I.3
  • 6
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    • Deletions of chromosome 15 as a cause of the Prader-Willi syndrome
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    • Ledbetter, D.H.1    Riccardi, V.M.2    Airhart, S.D.3
  • 7
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    • Nicholls RD. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review. Am J Med Genet 1993; 46:16-25.
    • (1993) Am J Med Genet , vol.46 , pp. 16-25
    • Nicholls, R.D.1
  • 8
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    • Nondisjunction of chromosome 15: Origin and recombination
    • Robinson WP, Bernasconi F, Mutirangura A, et al. Nondisjunction of chromosome 15: origin and recombination. Am J Hum Genet 1993; 53:740-51.
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  • 9
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.