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R C Trembath

Showing results (21-30 of 86) with videos related to

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The British Journal of Dermatology|May 1, 1994
An association between psoriasis and hereditary multiple exostoses. A clue for the mapping of a psoriasis susceptibility gene?J L Rosbotham, R C Trembath, M Glover, et al.
Journal of Medical Genetics|November 2, 1999
The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteriaS M Price, R Stanhope, C Garrett, et al.
Journal of Medical Genetics|December 6, 2005
Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorderE Kinning, C Tufarelli, W S Winship, et al.
QJM : Monthly Journal of the Association of Physicians|January 1, 1997
Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophyS N Jackson, T A Howlett, P G McNally, et al.
AIDS (London, England)|September 14, 2000
Lessons from lipodystrophy: LMNA, encoding lamin A/C, in HIV therapy-associated lipodystrophyG M Behrens, D Lloyd, H H Schmidt, et al.
Archives of Disease in Childhood|April 1, 1991
Nesidioblastosis: evidence for autosomal recessive inheritanceD A Woolf, J V Leonard, R C Trembath, et al.
Journal of Medical Genetics|February 1, 1997
Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosisL C Wilson, M E Oude Luttikhuis, M Baraitser, et al.
Clinical and Experimental Dermatology|July 28, 2005
Skin tumours and a family history of cancerM J Sladden, N J Mortimer, R D R Camp, et al.
British Medical Journal (Clinical Research Ed.)|June 20, 1987
Deoxyribonucleic acid polymorphism of the apoprotein AI-CIII-AIV gene cluster and coronary heart disease in non-insulin-dependent diabetesR C Trembath, D J Thomas, T J Hendra, et al.
Diabetologia|November 1, 1988
Linkage analysis of the human insulin receptor gene in type 2 (non-insulin-dependent) diabetic families and a family with maturity onset diabetes of the youngS O'Rahilly, R C Trembath, P Patel, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|May 1, 1994
An association between psoriasis and hereditary multiple exostoses. A clue for the mapping of a psoriasis susceptibility gene?J L Rosbotham, R C Trembath, M Glover, et al.
Journal of Medical Genetics|November 2, 1999
The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteriaS M Price, R Stanhope, C Garrett, et al.
Journal of Medical Genetics|December 6, 2005
Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorderE Kinning, C Tufarelli, W S Winship, et al.
QJM : Monthly Journal of the Association of Physicians|January 1, 1997
Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophyS N Jackson, T A Howlett, P G McNally, et al.
AIDS (London, England)|September 14, 2000
Lessons from lipodystrophy: LMNA, encoding lamin A/C, in HIV therapy-associated lipodystrophyG M Behrens, D Lloyd, H H Schmidt, et al.
Archives of Disease in Childhood|April 1, 1991
Nesidioblastosis: evidence for autosomal recessive inheritanceD A Woolf, J V Leonard, R C Trembath, et al.
Journal of Medical Genetics|February 1, 1997
Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosisL C Wilson, M E Oude Luttikhuis, M Baraitser, et al.
Clinical and Experimental Dermatology|July 28, 2005
Skin tumours and a family history of cancerM J Sladden, N J Mortimer, R D R Camp, et al.
British Medical Journal (Clinical Research Ed.)|June 20, 1987
Deoxyribonucleic acid polymorphism of the apoprotein AI-CIII-AIV gene cluster and coronary heart disease in non-insulin-dependent diabetesR C Trembath, D J Thomas, T J Hendra, et al.
Diabetologia|November 1, 1988
Linkage analysis of the human insulin receptor gene in type 2 (non-insulin-dependent) diabetic families and a family with maturity onset diabetes of the youngS O'Rahilly, R C Trembath, P Patel, et al.
Pageof 9