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Showing page 1 of results 1 - 5 of about 5 matches for "cangul-hakan"

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A Nonsense Thyrotropin Receptor Gene Mutation (R609X) is Associated with Congenital Hypothyroidism and Heart Defects*
Hakan Cangul; Veysel Nijat Bas; Yaman Saglam; Michaela Kendall; Timothy G Barrett; Eamonn R Maher; Zehra Aycan
http://abstracts.eurospe.org/hrp/0082/hrp0082p1-d1-235.htm
Published: 2014-08-28

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A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism
Nadia Schoenmakers; Hakan Cangul; Adeline K Nicholas; Erik Schoenmakers; Greta Lyons; Mehul Dattani; Catherine Peters; Shirley L
http://www.endocrine-abstracts.org/ea/0033/ea0033oc2.9.htm
Published: 2013-11-01

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Investigating the genetic architecture of gland-in-situ congenital hypothyroidism by comprehensive screening of eight known causative genes
Adeline K Nicholas; Eva Goncalves Serra; Hakan Cangul; Saif Al-Yaarubi; Irfan Ullah; Abdelhadi Habeb; Asma Deeb; Catherine Peter
http://www.endocrine-abstracts.org/ea/0038/ea0038oc5.5.htm
Published: 2015-10-12

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The Investigation of Genetic Etiology in Familial Cases with Congenital Hypothyroidism | ESPE2019
Al Asli Derya Kardelen; Fatma Büsra Isik; Esin Karakiliç Özturan; Mavi Deniz Sözügüzel; Ayse Pinar Öztürk; Sükran Poyra
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-145
Published: 2019-08-22

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The Investigation of Genetic Etiology in Familial Cases with Congenital Hypothyroidism | ESPE2019
Al Asli Derya Kardelen; Fatma Büsra Isik; Esin Karakiliç Özturan; Mavi Deniz Sözügüzel; Ayse Pinar Öztürk; Sükran Poyra
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-145.html
Published: 2019-08-22

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