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J Weissenbach

Showing results (151-160 of 363) with videos related to

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Human Molecular Genetics|January 1, 1994
The gene for Darier's disease maps between D12S78 and D12S79E Parfitt, S Burge, N Craddock, et al.
Cancer Research|November 1, 1995
Loss of the chromosomal region 10q23-25 in prostate cancerI C Gray, S M Phillips, S J Lee, et al.
Human Molecular Genetics|June 1, 1994
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 geneP Guilford, H Ayadi, S Blanchard, et al.
Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.
Psychiatric Genetics|July 1, 1997
A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking familiesB P Riley, E Tahir, S Rajagopalan, et al.
Blood|November 15, 1995
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1H Cavé, B Gérard, E Martin, et al.
Journal of Medical Genetics|September 1, 1996
Clinical and genetic heterogeneity of hypochondroplasiaF Rousseau, J Bonaventure, L Legeai-Mallet, et al.
Science (New York, N.Y.)|December 20, 1985
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distanceM Casanova, P Leroy, C Boucekkine, et al.
Genomics|March 20, 1995
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysisE Tahvanainen, H Forsius, E Karila, et al.
Human Molecular Genetics|January 1, 1997
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21H Chaïb, J Kaplan, S Gerber, et al.
Pageof 37

Showing results (151-160 of 363) with videos related to

Sort By:
Pageof 37
Human Molecular Genetics|January 1, 1994
The gene for Darier's disease maps between D12S78 and D12S79E Parfitt, S Burge, N Craddock, et al.
Cancer Research|November 1, 1995
Loss of the chromosomal region 10q23-25 in prostate cancerI C Gray, S M Phillips, S J Lee, et al.
Human Molecular Genetics|June 1, 1994
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 geneP Guilford, H Ayadi, S Blanchard, et al.
Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.
Psychiatric Genetics|July 1, 1997
A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking familiesB P Riley, E Tahir, S Rajagopalan, et al.
Blood|November 15, 1995
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1H Cavé, B Gérard, E Martin, et al.
Journal of Medical Genetics|September 1, 1996
Clinical and genetic heterogeneity of hypochondroplasiaF Rousseau, J Bonaventure, L Legeai-Mallet, et al.
Science (New York, N.Y.)|December 20, 1985
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distanceM Casanova, P Leroy, C Boucekkine, et al.
Genomics|March 20, 1995
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysisE Tahvanainen, H Forsius, E Karila, et al.
Human Molecular Genetics|January 1, 1997
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21H Chaïb, J Kaplan, S Gerber, et al.
Pageof 37