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- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q
- Prenatal serological diagnosis of intrauterine cytomegalovirus infection.
- Prenatal Screening for Bathing-suit Ichthyosis After Diagnosis in an Older Sibling
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
- PCOS: update and diagnostic approach
- Inherited ichthyosis: Syndromic forms
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
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