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Showing page 1 of results 1 - 6 of about 6 pages

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Growth Hormone (GH) Deficiency Type II: Clinical and Molecular Evidence of Impaired Regulated GH Secretion Due to an Gln181Arg GH-1 Gene Mutation | ESPE2016
Maria Consolata Miletta; Andree Eble; Ivo J P Arnhold; Andrew Dauber; Christa Fluck; Amit Pandey
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc6.6.htm
Published: 2016-08-19

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Genetic Causes of Disproportional Short Stature Identified by Whole Exome Sequencing | ESPE2015
Mariana F A Funari; Gabriela A Vasques; Antonio M Lerario; Bruna L Freire; Mirian Y Nishi; Monica M Franca; Sueli M O Shinjo; Su
http://abstracts.eurospe.org/hrp/0084/hrp0084lbp-1268.htm
Published: 2015-08-26

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Birth Characteristics Influence the Male to Female Diagnostic Prevalence of Idiopathic GH Deficiency | ESPE2015
Cecilia Camacho-Hubner; Anders Lindberg; Ivo J P Arnhold; Michael B Ranke
http://abstracts.eurospe.org/hrp/0084/hrp0084p3-1034.htm
Published: 2015-08-26

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GH Deficiency with Advanced Bone Age: GHRH Receptor Mutation Detected by Exome Sequencing Associated to Non-Classical Congenital Adrenal Hyperplasia (CAH) | ESPE2015
Fernanda de Azevedo Correa; Marcela M Franca; Qing Fang; Qianyi Ma; Tania A Bachega; Berenice B Mendonca; Alexander LJorge; Luci
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-535.htm
Published: 2015-08-26

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Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes | ESPE2015
Fernanda A Correa; Marcela M Franca; Ana P M Canton; Aline P Otto; Everlayny F Costalonga; Vinicius N Brito; Luciani R Carvalho;
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-523.htm
Published: 2015-08-26

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Characterisation of Mutations in the Androgen Receptor Identified in 38 Brazilian Families with Complete or Partial Androgen Insensitivity Syndrome | ESPE2015
Rafael Loch Batista; Andreza Santi; Ivo J P Arnhold; Flavia S Cunha; Elaine M F Costa; Berenince B Mendonca; Sorahia Domenice
http://abstracts.eurospe.org/hrp/0084/hrp0084fc6.5.htm
Published: 2015-08-26

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