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R C Trembath

Showing results (51-60 of 86) with videos related to

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The British Journal of Dermatology|August 15, 2009
Genetic analysis of desmoglein 3 (DSG3) sequence variants in patients with pemphigus vulgarisF Capon, H Boulding, M Quaranta, et al.
Diabetes|June 1, 1994
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) geneJ M van den Ouweland, H H Lemkes, R C Trembath, et al.
Scientifica|November 27, 2013
A Novel ABCA12 Mutation in Two Families with Congenital IchthyosisD M Walsh, S H Shah, M A Simpson, et al.
The British Journal of Dermatology|April 16, 1998
Association of atopic dermatitis to the beta subunit of the high affinity immunoglobulin E receptorH E Cox, M F Moffatt, J A Faux, et al.
Gut|February 1, 1993
Effect of octreotide on gall stone prevalence and gall bladder motility in acromegalyS M Catnach, J V Anderson, P D Fairclough, et al.
American Journal of Human Genetics|July 31, 1998
A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1qS N Jackson, J Pinkney, A Bargiotta, et al.
Journal of Medical Genetics|September 3, 2002
Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)I A Aligianis, T Forshew, S Johnson, et al.
Nature Genetics|September 6, 2000
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension, K B Lane, R D Machado, et al.
The British Journal of Dermatology|July 29, 2016
Hidradenitis suppurativa: haploinsufficiency of gamma-secretase components does not affect gamma-secretase enzyme activity in vitroA E Pink, D Dafou, N Desai, et al.
Journal of Medical Genetics|June 17, 2003
Haplotype analysis of distantly related populations implicates corneodesmosin in psoriasis susceptibilityF Capon, I K Toal, J C Evans, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|August 15, 2009
Genetic analysis of desmoglein 3 (DSG3) sequence variants in patients with pemphigus vulgarisF Capon, H Boulding, M Quaranta, et al.
Diabetes|June 1, 1994
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) geneJ M van den Ouweland, H H Lemkes, R C Trembath, et al.
Scientifica|November 27, 2013
A Novel ABCA12 Mutation in Two Families with Congenital IchthyosisD M Walsh, S H Shah, M A Simpson, et al.
The British Journal of Dermatology|April 16, 1998
Association of atopic dermatitis to the beta subunit of the high affinity immunoglobulin E receptorH E Cox, M F Moffatt, J A Faux, et al.
Gut|February 1, 1993
Effect of octreotide on gall stone prevalence and gall bladder motility in acromegalyS M Catnach, J V Anderson, P D Fairclough, et al.
American Journal of Human Genetics|July 31, 1998
A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1qS N Jackson, J Pinkney, A Bargiotta, et al.
Journal of Medical Genetics|September 3, 2002
Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)I A Aligianis, T Forshew, S Johnson, et al.
Nature Genetics|September 6, 2000
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension, K B Lane, R D Machado, et al.
The British Journal of Dermatology|July 29, 2016
Hidradenitis suppurativa: haploinsufficiency of gamma-secretase components does not affect gamma-secretase enzyme activity in vitroA E Pink, D Dafou, N Desai, et al.
Journal of Medical Genetics|June 17, 2003
Haplotype analysis of distantly related populations implicates corneodesmosin in psoriasis susceptibilityF Capon, I K Toal, J C Evans, et al.
Pageof 9