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Molecular characterization in a case of isolated growth hormone deficiency and further prenatal diagnosis of an unborn sibling.
Indian J Hum Genet ; 2013 Oct-Dec ;19 (4): 475-478
Article in En | IMSEAR | ID: sea-156618
Full text: 1 Index: IMSEAR Main subject: Prenatal Diagnosis / Humans / Male / Polymerase Chain Reaction / Gene Deletion / Human Growth Hormone / Siblings / Fetus / Growth Disorders / Infant Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Indian J Hum Genet Year: 2013 Type: Article
Full text: 1 Index: IMSEAR Main subject: Prenatal Diagnosis / Humans / Male / Polymerase Chain Reaction / Gene Deletion / Human Growth Hormone / Siblings / Fetus / Growth Disorders / Infant Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Indian J Hum Genet Year: 2013 Type: Article