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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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L Papi

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Human Molecular Genetics|March 1, 1993

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.

Human Genetics|May 1, 1996

Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal originL R De Vitis, A Tedde, F Vitelli, et al.

Nature|June 3, 1993

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.

Journal of Medical Genetics|July 5, 2005

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2M E Baser, L Kuramoto, R Woods, et al.

American Journal of Medical Genetics. Part A|October 21, 2016

Creation of an international registry to support discovery in schwannomatosisK L Ostrow, A L Bergner, J Blakeley, et al.

Human Molecular Genetics|February 13, 2001

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGHC E Bruder, C Hirvelä, I Tapia-Paez, et al.

Pageof 5

Search research articles

Showing results (41-50 of 46) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 46 results.

Human Molecular Genetics|March 1, 1993

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.

Human Genetics|May 1, 1996

Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal originL R De Vitis, A Tedde, F Vitelli, et al.

Nature|June 3, 1993

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.

Journal of Medical Genetics|July 5, 2005

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2M E Baser, L Kuramoto, R Woods, et al.

American Journal of Medical Genetics. Part A|October 21, 2016

Creation of an international registry to support discovery in schwannomatosisK L Ostrow, A L Bergner, J Blakeley, et al.

Human Molecular Genetics|February 13, 2001

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGHC E Bruder, C Hirvelä, I Tapia-Paez, et al.

Pageof 5