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ullar imath
ullar imath
Genetics
Mutation (genetic algorithm)
Medicine
expressivity
Growth hormone receptor
3
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2024
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Retrospective Evaluation of Cases Diagnosed with Classical Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Deficiency
2021
Nafiye Unsal
Selin Elmao gbreve
ullar imath
Erdeve Senay Savas
Semra Çetinkaya
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A Rare Cause of Familial Hypomagnesemia: A Case with Trpm6 Mutation
2021
Merve Sakar
Semra Çetinkaya
Kücukali Gülin Karacan
Şervan Özalkak
Selin Elmao gbreve
ullar imath
Şahin Nursel Murato gbreve
Lu
Melikşah Keskin
Naz Guleray Lafc imath
Erdeve Senay Savas
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Two Sibling Cases with Growth Hormone Receptor Mutation: Variable Clinical Expressivity in Laron Syndrome
2021
Ozdemir Behiye Sar imath
Kaya
Semra Çetinkaya
Lafc imath
Naz Güleray
Merve Sakar
Gülin Karacan Küçükali
Selin Elmao gbreve
ullar imath
Erdeve Senay Savas
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