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- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome
- Bloom's syndrome–‐a first report from India
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Primary Amenorrhoea
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Frontal Fibrosing Alopecia
- Marie-unna hereditary hypotrichosis
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
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