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Publications by Sulman Basit

Linkage Analysis Coupled With Exome Sequencing Identified Defects in Gene ‘X’ Causing Premature Ovarian Insufficiency

English

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Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

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Occult Form of Premature Ovarian Insufficiency

Gynecological Endocrinology

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Exome Sequencing Identified New Mutations in a Marfan Syndrome Family

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Forensic Medicine

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Adolescent Premature Ovarian Insufficiency Following Human Papillomavirus Vaccination

Journal of Investigative Medicine High Impact Case Reports

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Premature Ovarian Insufficiency – To Treat or Not to Treat?

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Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

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A Rare ANOS1 Variant in Siblings With Kallmann Syndrome Identified by Whole Exome Sequencing

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Identification of ADHD Risk Genes in Extended Pedigrees by Combining Linkage Analysis and Whole-Exome Sequencing

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Premature Ovarian Insufficiency: Step-By-Step, Genetics Bring New Insights

Fertility and Sterility

Reproductive Medicine

English