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M E Pembrey

Showing results (91-100 of 99) with videos related to

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American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.
British Medical Journal (Clinical Research Ed.)|September 21, 1985
First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13R M Winter, K Harper, E Goldman, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.
Nature Genetics|May 20, 1998
Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and ChildhoodD B Dunger, K K Ong, S J Huxtable, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1998
Neural basis of an inherited speech and language disorderF Vargha-Khadem, K E Watkins, C J Price, et al.
Journal of Medical Genetics|February 1, 1997
Pendred syndrome: evidence for genetic homogeneity and further refinement of linkageE Gausden, B Coyle, J A Armour, et al.
Clinical Radiology|May 19, 1998
Radiological malformations of the ear in Pendred syndromeP D Phelps, R A Coffey, R C Trembath, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.
British Medical Journal (Clinical Research Ed.)|September 21, 1985
First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13R M Winter, K Harper, E Goldman, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.
Nature Genetics|May 20, 1998
Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and ChildhoodD B Dunger, K K Ong, S J Huxtable, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1998
Neural basis of an inherited speech and language disorderF Vargha-Khadem, K E Watkins, C J Price, et al.
Journal of Medical Genetics|February 1, 1997
Pendred syndrome: evidence for genetic homogeneity and further refinement of linkageE Gausden, B Coyle, J A Armour, et al.
Clinical Radiology|May 19, 1998
Radiological malformations of the ear in Pendred syndromeP D Phelps, R A Coffey, R C Trembath, et al.
Pageof 10