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Spectrum of mutations in cystinuria patients presenting with prenatal hyperechoic colon.
Tostivint, I; Royer, N; Nicolas, M; Bourillon, A; Czerkiewicz, I; Becker, P-H; Muller, F; Benoist, J-F.
Afiliação
  • Tostivint I; Department of Urology and Nephrology, Interdisciplinary Urolithiasis Center, Pitié-Salpêtrière Universitary Teaching Hospital, Paris, France.
  • Royer N; Service de Biochimie Hormonologie, APHP, Paris, France.
  • Nicolas M; Service de Biochimie Hormonologie, APHP, Paris, France.
  • Bourillon A; Service de Biochimie Hormonologie, APHP, Paris, France.
  • Czerkiewicz I; Service de Biochimie Hormonologie, APHP, Paris, France.
  • Becker PH; Service de Biochimie Hormonologie, APHP, Paris, France.
  • Muller F; Service de Biochimie Hormonologie, APHP, Paris, France.
  • Benoist JF; Service de Biochimie Hormonologie, APHP, Paris, France.
Clin Genet ; 92(6): 632-638, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28646536
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2017 Tipo de documento: Article