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A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.

机译：一项在prokineticin 2或prokineticin receptor 2基因中携带单等位基因和双等位基因突变的kallmann综合征患者的比较表型研究。

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Sarfati, Julie; Guiochon-Mantel, Anne; Rondard, Philippe; Arnulf, Isabelle; Garcia-Piñero, Alfons; Wolczynski, Slawomir; Brailly-Tabard, Sylvie; Bidet, Maud; Ramos-Arroyo, Maria; Mathieu, Michèle; Lienhardt-Roussie, Anne; Morgan, Graeme; Turki, Zinet; Bremont, Catherine; Lespinasse, James; Du Boullay, Hélène; Chabbert-Buffet, Nathalie; Jacquemont, Sébastien; Reach, Gérard; De Talence, Nicole; Tonella, Paolo; Conrad, Bernard; Despert, Francois; Delobel, Bruno; Brue, Thierry; Bouvattier, Claire; Cabrol, Sylvie; Pugeat, Michel; Murat, Arnaud; Bouchard, Philippe; Hardelin, Jean-Pierre; Dodé, Catherine; Young, Jacques;
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1. A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes [J] . Julie Sarfati, Anne Guiochon-Mantel, Philippe Rondard, The journal of clinical endocrinology and metabolism . 2010,第2期

机译：携带Prokineticin 2或Prokineticin Receptor 2基因的单等位基因和双等位基因突变的Kallmann综合征患者的比较表型研究
2. Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 [J] . Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, PLoS Genetics . 2006,第10期

机译：Kallmann综合征：编码Prokineticin-2和Prokineticin Receptor-2的基因中的突变。
3. Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome. [J] . Leroy C, Fouveaut C, Leclercq S, European journal of human genetics: EJHG . 2008,第7期

机译：在两个散发性Kallmann综合征病例中prokineticin-2基因的双等位基因突变。
4. The E1784K mutation in SCN5A and phenotypic overlap of Type 3 Long QT syndrome and Brugada syndrome: A simulation study [C] . Wang K.Q., Yuan Y.F., Kharche S., Computers in Cardiology, 2009 . 2009

机译：模拟研究3型长QT综合征和Brugada综合征的SCN5A中的E1784K突变和表型重叠
5. Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 [O] . Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, 2006

机译：Kallmann综合征：编码Prokineticin-2和Prokineticin Receptor-2的基因中的突变。
6. A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes. [O] . Sarfati, Julie, Guiochon-Mantel, Anne, Rondard, Philippe, 2010

机译：一项在prokineticin 2或prokineticin receptor 2基因中携带单等位基因和双等位基因突变的kallmann综合征患者的比较表型研究。

A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.

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