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M E Pembrey

Showing results (81-90 of 99) with videos related to

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Journal of Medical Genetics|November 1, 1991
Microtia and short stature: a new syndromeB Cohen, I K Temple, J C Symons, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Lancet (London, England)|February 20, 1988
Risk estimation and screening in families of patients with medullary thyroid carcinomaB A Ponder, M A Ponder, R Coffey, et al.
British Journal of Audiology|April 1, 1992
Clinical and genetic heterogeneity in X-linked deafnessW Reardon, H R Middleton-Price, S Malcolm, et al.
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Journal of Medical Genetics|August 1, 1997
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome familiesH L Gilbert, J L Buxton, C T Chan, et al.
The Quarterly Journal of Medicine|April 1, 1988
Family screening in medullary thyroid carcinoma presenting without a family historyB A Ponder, N Finer, R Coffey, et al.
Cell|July 16, 1993
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardationS J Knight, A V Flannery, M C Hirst, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|November 1, 1991
Microtia and short stature: a new syndromeB Cohen, I K Temple, J C Symons, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
American Journal of Medical Genetics|September 15, 1992
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndromeJ Clayton-Smith, T Webb, S A Robb, et al.
Lancet (London, England)|February 20, 1988
Risk estimation and screening in families of patients with medullary thyroid carcinomaB A Ponder, M A Ponder, R Coffey, et al.
British Journal of Audiology|April 1, 1992
Clinical and genetic heterogeneity in X-linked deafnessW Reardon, H R Middleton-Price, S Malcolm, et al.
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Journal of Medical Genetics|August 1, 1997
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome familiesH L Gilbert, J L Buxton, C T Chan, et al.
The Quarterly Journal of Medicine|April 1, 1988
Family screening in medullary thyroid carcinoma presenting without a family historyB A Ponder, N Finer, R Coffey, et al.
Cell|July 16, 1993
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardationS J Knight, A V Flannery, M C Hirst, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
Pageof 10