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Volumn 5, Issue 2, 2012, Pages 218-220

A rare cause for primary amenorrhoea

Author keywords

Deafness; karyotype; marfanoid habitus; ovarian dysgenesis; Perrault's syndrome

Indexed keywords

ANTIDEPRESSANT AGENT; ELECTROLYTE; ESTRADIOL; ESTROGEN; FOLLITROPIN; GLUCOSE; LUTEINIZING HORMONE; PROGESTERONE; TESTOSTERONE;

EID: 84866657907     PISSN: 09741208     EISSN: 19984766     Source Type: Journal    
DOI: 10.4103/0974-1208.101026     Document Type: Article
Times cited : (2)

References (13)
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    • Cruz, O.L.1    Pedalini, M.E.2    Caropreso, C.A.3
  • 10
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    • Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome
    • Pierce SB, Walsh T, Chisholm KM, Lee MK, Thornton AM, Fiumara A, et al. Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. Am J Hum Genet 2011;87:282-8.
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    • Pierce, S.B.1    Walsh, T.2    Chisholm, K.M.3    Lee, M.K.4    Thornton, A.M.5    Fiumara, A.6
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    • Wilson W, Taubert KA, Gewitz M, Lockhart PB, Baddour LM, Levison M et al. Prevention of infective endocarditis: Guidelines from the American Heart Association: A guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery andAnesthesia, and the Quality of Care and Outcomes Research InterdisciplinaryWorking Group. Circulation 2007;116:1736-54.
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  • 12
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    • ACC/AHA2008 guideline update on valvular heart disease: Focused update on infective endocarditis: A report of the American College of Cardiology/American HeartAssociation Task Force on Practice Guidelines
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    • The Perrault syndrome: Autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafness
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    • Pallister, P.D.1    Opitz, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.