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syndrome genetic
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Most Correlated Studies
OMIM - Congenital disorder
OMIM - Watson syndrome
Brains and skeletal muscles of Prader-Will syndrome imprinting center (PWS-IC) deleted mice
Pluripotent stem cells and myeloid cells derived and differentiated from Noonan syndrome patients
Induced pluripotent stem cells (iPSCs) and fibroblasts of patients with Prader-Willi syndrome
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Long QT syndrome - a genetic cardiac channelopathy.
The genetics of Tourette syndrome.
Extracorporeal membrane oxygenation in children with heart disease and genetic syndromes.
Autism spectrum disorders: the quest for genetic syndromes.
Genetic testing in nephrotic syndrome--challenges and opportunities.
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Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan
Acute Coronary Syndrome Genetic Study
A Study to Characterize Epidemiology, Clinical and Genetic Features of Kallmann Syndrome in Finland
Scleral Buckling for Retinal Detachment Prevention in Genetically Confirmed Stickler Syndrome
Genetic Analysis of Oculocerebrorenal Syndrome of Lowe
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