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Ian Carr

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Molecular Vision|November 7, 2013

A new recessively inherited disorder composed of foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis maps to chromosome 16q23.3-24.1Musallam Al-Araimi, Bishwanath Pal, James A Poulter, et al.

The Journal of Clinical Endocrinology and Metabolism|January 29, 2025

Endocrine alterations in patients with pachydermoperiostosisMaria Stelmachowska-Banaś, Sayka Barry, Ishita Angurala, et al.

American Journal of Human Genetics|September 3, 2011

Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyteDavid A Parry, Clare V Logan, Bruce E Hayward, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 13 results.

Molecular Vision|November 7, 2013

The Journal of Clinical Endocrinology and Metabolism|January 29, 2025

Endocrine alterations in patients with pachydermoperiostosisMaria Stelmachowska-Banaś, Sayka Barry, Ishita Angurala, et al.

American Journal of Human Genetics|September 3, 2011

Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyteDavid A Parry, Clare V Logan, Bruce E Hayward, et al.

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