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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Nisha Limaye

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Human Genetics|April 3, 2008

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.

Human Genetics|April 3, 2008

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.

The Journal of Investigative Dermatology|August 14, 2016

Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) MutationsJulie Soblet, Jaakko Kangas, Marjut Nätynki, et al.

Nature Genetics|November 8, 2011

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeTwinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.

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Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 44 results.

Human Genetics|April 3, 2008

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.

Human Genetics|April 3, 2008

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.

The Journal of Investigative Dermatology|August 14, 2016

Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) MutationsJulie Soblet, Jaakko Kangas, Marjut Nätynki, et al.

Nature Genetics|November 8, 2011

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeTwinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.

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