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C C Morton

Showing results (141-150 of 185) with videos related to

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Genomics|June 30, 2000
A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mappingN G Robertson, S Heller, J S Lin, et al.
The Journal of Biological Chemistry|September 25, 1998
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defectsH Nomura, A E Turco, Y Pei, et al.
The New England Journal of Medicine|February 14, 1991
Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumorsJ A Fletcher, H P Kozakewich, F A Hoffer, et al.
Genomics|August 1, 1996
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130C T Basson, C A MacRae, M Schoenberg-Fejzo, et al.
Human Mutation|January 1, 1997
Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiencyH L Rehm, G A Gutiérrez-Espeleta, R Garcia, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Assignment of C1QBP encoding the C1q globular domain binding protein (gC1q-R) to human chromosome 17 band p13.3 by in situ hybridizationN Guo, S Weremowicz, N Lynch, et al.
American Journal of Human Genetics|April 1, 1991
A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPsR L Maas, L I Jepeal, S L Elfering, et al.
American Journal of Mental Deficiency|March 1, 1984
Molecular genetic approaches to human diseases involving mental retardationS A Latt, D M Kurnit, G P Bruns, et al.
Diabetes|February 1, 1995
Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16qA Doria, J S Caldwell, L Ji, et al.
Human Molecular Genetics|February 13, 2001
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, et al.
Pageof 19

Showing results (141-150 of 185) with videos related to

Sort By:
Pageof 19
Genomics|June 30, 2000
A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mappingN G Robertson, S Heller, J S Lin, et al.
The Journal of Biological Chemistry|September 25, 1998
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defectsH Nomura, A E Turco, Y Pei, et al.
The New England Journal of Medicine|February 14, 1991
Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumorsJ A Fletcher, H P Kozakewich, F A Hoffer, et al.
Genomics|August 1, 1996
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130C T Basson, C A MacRae, M Schoenberg-Fejzo, et al.
Human Mutation|January 1, 1997
Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiencyH L Rehm, G A Gutiérrez-Espeleta, R Garcia, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Assignment of C1QBP encoding the C1q globular domain binding protein (gC1q-R) to human chromosome 17 band p13.3 by in situ hybridizationN Guo, S Weremowicz, N Lynch, et al.
American Journal of Human Genetics|April 1, 1991
A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPsR L Maas, L I Jepeal, S L Elfering, et al.
American Journal of Mental Deficiency|March 1, 1984
Molecular genetic approaches to human diseases involving mental retardationS A Latt, D M Kurnit, G P Bruns, et al.
Diabetes|February 1, 1995
Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16qA Doria, J S Caldwell, L Ji, et al.
Human Molecular Genetics|February 13, 2001
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, et al.
Pageof 19