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Human Molecular Genetics|October 23, 1997

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.

Clinical Genetics|October 27, 2015

Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.

Clinical Genetics|November 20, 2015

Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.

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Search research articles

Showing results (61-70 of 63) with videos related to

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You have reached the last page of results.This site can display upto 63 results.

Human Molecular Genetics|October 23, 1997

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.

Clinical Genetics|October 27, 2015

Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.

Clinical Genetics|November 20, 2015

Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.

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