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A P Read

Showing results (41-50 of 102) with videos related to

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Nature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.
Lancet (London, England)|July 19, 1986
Possible maternal effect in genetic susceptibility to myasthenia gravisA P Read, L Kerzin-Storrar, P A Dyer, et al.
Cancer Research|December 15, 1994
Deletion mapping on the short arm of chromosome 3 in squamous cell carcinoma of the oral cavityC L Wu, P Sloan, A P Read, et al.
British Medical Journal|November 8, 1980
Haemangioma of the cord: further cause of raised maternal serum and liquor alpha-fetoproteinA J Barson, P Donnai, A Ferguson, et al.
Neuromuscular Disorders : NMD|January 1, 1991
X-linked and FSH dystrophies in one familyB R Lecky, J M MacKenzie, A P Read, et al.
European Journal of Human Genetics : EJHG|May 30, 2003
Mutations in PAX1 may be associated with Klippel-Feil syndromeJ M McGaughran, A Oates, D Donnai, et al.
Journal of Medical Genetics|July 1, 1990
Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?R G Elles, A P Read, K A Hodgkinson, et al.
American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.
Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndromeM Tassabehji, M Carette, C Wilmot, et al.
Pageof 11

Showing results (41-50 of 102) with videos related to

Sort By:
Pageof 11
Nature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.
Lancet (London, England)|July 19, 1986
Possible maternal effect in genetic susceptibility to myasthenia gravisA P Read, L Kerzin-Storrar, P A Dyer, et al.
Cancer Research|December 15, 1994
Deletion mapping on the short arm of chromosome 3 in squamous cell carcinoma of the oral cavityC L Wu, P Sloan, A P Read, et al.
British Medical Journal|November 8, 1980
Haemangioma of the cord: further cause of raised maternal serum and liquor alpha-fetoproteinA J Barson, P Donnai, A Ferguson, et al.
Neuromuscular Disorders : NMD|January 1, 1991
X-linked and FSH dystrophies in one familyB R Lecky, J M MacKenzie, A P Read, et al.
European Journal of Human Genetics : EJHG|May 30, 2003
Mutations in PAX1 may be associated with Klippel-Feil syndromeJ M McGaughran, A Oates, D Donnai, et al.
Journal of Medical Genetics|July 1, 1990
Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?R G Elles, A P Read, K A Hodgkinson, et al.
American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.
Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndromeM Tassabehji, M Carette, C Wilmot, et al.
Pageof 11