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U Radhakrishna

Showing results (11-20 of 23) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|January 23, 2020
Artificial neural networks allow response prediction in squamous cell carcinoma of the scalp treated with radiotherapyG Damiani, E Grossi, E Berti, et al.
American Journal of Medical Genetics|July 11, 1997
The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric regionU Radhakrishna, J L Blouin, H Mehenni, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 3, 2022
Methylated miRNAs may serve as potential biomarkers and therapeutic targets for hidradenitis suppurativaU Radhakrishna, U Ratnamala, D D Jhala, et al.
Molecular Human Reproduction|August 5, 2006
Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26C Ravel, B El Houate, S Chantot, et al.
American Journal of Human Genetics|December 18, 1997
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4H Mehenni, J L Blouin, U Radhakrishna, et al.
American Journal of Human Genetics|August 12, 1999
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutationsU Radhakrishna, D Bornholdt, H S Scott, et al.
American Journal of Medical Genetics|April 17, 1999
No evidence for linkage between schizophrenia and markers at chromosome 15q13-14L Curtis, J L Blouin, U Radhakrishna, et al.
American Journal of Human Genetics|January 3, 2001
Y-chromosome lineages trace diffusion of people and languages in southwestern AsiaL Quintana-Murci, C Krausz, T Zerjal, et al.
American Journal of Medical Genetics|July 14, 1999
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21S E Antonarakis, J L Blouin, V K Lasseter, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mappingZ Kibar, M P Dubé, J Powell, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

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Pageof 3
Journal of the European Academy of Dermatology and Venereology : JEADV|January 23, 2020
Artificial neural networks allow response prediction in squamous cell carcinoma of the scalp treated with radiotherapyG Damiani, E Grossi, E Berti, et al.
American Journal of Medical Genetics|July 11, 1997
The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric regionU Radhakrishna, J L Blouin, H Mehenni, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 3, 2022
Methylated miRNAs may serve as potential biomarkers and therapeutic targets for hidradenitis suppurativaU Radhakrishna, U Ratnamala, D D Jhala, et al.
Molecular Human Reproduction|August 5, 2006
Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26C Ravel, B El Houate, S Chantot, et al.
American Journal of Human Genetics|December 18, 1997
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4H Mehenni, J L Blouin, U Radhakrishna, et al.
American Journal of Human Genetics|August 12, 1999
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutationsU Radhakrishna, D Bornholdt, H S Scott, et al.
American Journal of Medical Genetics|April 17, 1999
No evidence for linkage between schizophrenia and markers at chromosome 15q13-14L Curtis, J L Blouin, U Radhakrishna, et al.
American Journal of Human Genetics|January 3, 2001
Y-chromosome lineages trace diffusion of people and languages in southwestern AsiaL Quintana-Murci, C Krausz, T Zerjal, et al.
American Journal of Medical Genetics|July 14, 1999
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21S E Antonarakis, J L Blouin, V K Lasseter, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mappingZ Kibar, M P Dubé, J Powell, et al.
Pageof 3