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A Novel Mutation H373Y in the Wilms' Tumor Suppressor Gene, WT1, Associated with Denys-Drash Syndrome
by
Ghahremani, Majid
,
Chan, Chi-Bew
,
Bistritzer, Tzvy
,
Aladjem, M. Mordechai
,
Tiederh, Martin
,
Pelletier, Jerry
Published in
Human heredity
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Human Heredity
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Child, Preschool
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Disorders Of Sex Development - Genetics
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Genes, Wilms Tumor
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Genetics & Heredity
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Histidine - Genetics
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Humans
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Life Sciences & Biomedicine
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Male
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Mutation Report
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Nephrotic Syndrome - Genetics
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Point Mutation
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Polymerase Chain Reaction
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Polymorphism, Single-Stranded Conformational
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Tyrosine - Genetics
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