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Showing results (11-20 of 15) with videos related to

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Journal of Medical Genetics|February 1, 1997
Bardet-Biedl syndrome: a molecular and phenotypic study of 18 familiesP L Beales, A M Warner, G A Hitman, et al.
American Journal of Medical Genetics|March 29, 1996
Two sibs with anophthalmia and pulmonary hypoplasia (the Matthew-Wood syndrome)M J Seller, T B Davis, C N Fear, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 30, 2000
Renal cancer and malformations in relatives of patients with Bardet-Biedl syndromeP L Beales, H A Reid, M H Griffiths, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1999
Renal chloride channel, CLCN5, mutations in Dent's diseaseJ P Cox, K Yamamoto, P T Christie, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Journal of Medical Genetics|February 1, 1997
Bardet-Biedl syndrome: a molecular and phenotypic study of 18 familiesP L Beales, A M Warner, G A Hitman, et al.
American Journal of Medical Genetics|March 29, 1996
Two sibs with anophthalmia and pulmonary hypoplasia (the Matthew-Wood syndrome)M J Seller, T B Davis, C N Fear, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 30, 2000
Renal cancer and malformations in relatives of patients with Bardet-Biedl syndromeP L Beales, H A Reid, M H Griffiths, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1999
Renal chloride channel, CLCN5, mutations in Dent's diseaseJ P Cox, K Yamamoto, P T Christie, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Pageof 2