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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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R R Lebel

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Clinical Genetics|April 10, 2002

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.

American Journal of Medical Genetics|December 1, 1993

Model consent forms for DNA linkage analysis and storageR L Gold, R R Lebel, E A Mearns, et al.

Wisconsin Medical Journal|February 1, 1994

DNA testing and genetic counseling: truth or consequencesN C Reynolds, R R Lebel, K de S Hamsher, et al.

American Journal of Medical Genetics|April 1, 1984

Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomaliesB R Elejalde, J M Opitz, M M de Elejalde, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001

Duty to re-contactK Hirschhorn, L D Fleisher, L Godmilow, et al.

Human Molecular Genetics|February 1, 1996

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.

Clinical Genetics|April 23, 2016

Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotypingJ S Amos, L Huang, J Thevenon, et al.

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Search research articles

Showing results (21-30 of 27) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 27 results.

Clinical Genetics|April 10, 2002

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.

American Journal of Medical Genetics|December 1, 1993

Model consent forms for DNA linkage analysis and storageR L Gold, R R Lebel, E A Mearns, et al.

Wisconsin Medical Journal|February 1, 1994

DNA testing and genetic counseling: truth or consequencesN C Reynolds, R R Lebel, K de S Hamsher, et al.

American Journal of Medical Genetics|April 1, 1984

Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomaliesB R Elejalde, J M Opitz, M M de Elejalde, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001

Duty to re-contactK Hirschhorn, L D Fleisher, L Godmilow, et al.

Human Molecular Genetics|February 1, 1996

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.

Clinical Genetics|April 23, 2016

Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotypingJ S Amos, L Huang, J Thevenon, et al.

Pageof 3