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J Weissenbach

Showing results (101-110 of 363) with videos related to

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Cell|June 5, 1987
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX malenessC Petit, A de la Chapelle, J Levilliers, et al.
Nature|January 23, 1986
A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomesF Rouyer, M C Simmler, C Johnsson, et al.
American Journal of Human Genetics|March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisisS Saunier, J Calado, F Benessy, et al.
Genomics|October 10, 1995
Physical mapping of the human ELA1 gene between D12S361 and D12S347 on chromosome 12q13R L Davies, S J Yoon, J Weissenbach, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|March 1, 1995
Establishment of the marker order pter-NRAS-NGFB-D1S189-D1S252-D1S440-D1S453-D1S514-CEN-D1S442-D1S498-qte r in relation to the centromere on human chromosome 1N Hoggard, B Brintnell, Y Hey, et al.
Human Molecular Genetics|August 1, 1995
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneityL Parmentier, C Blanchet-Bardon, S Nguyen, et al.
American Journal of Human Genetics|October 1, 1995
Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17pR Goliath, Y Shugart, P Janssens, et al.
Human Genetics|April 1, 1998
Linkage between atopy and the IgE high-affinity receptor gene at 11q13 in atopic dermatitis familiesR Fölster-Holst, H W Moises, L Yang, et al.
American Journal of Human Genetics|January 1, 1995
Refining the localization of the PKD2 locus on chromosome 4q by linkage analysis in Spanish families with autosomal dominant polycystic kidney disease type 2J L San Millán, M Viribay, B Peral, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
Pageof 37

Showing results (101-110 of 363) with videos related to

Sort By:
Pageof 37
Cell|June 5, 1987
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX malenessC Petit, A de la Chapelle, J Levilliers, et al.
Nature|January 23, 1986
A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomesF Rouyer, M C Simmler, C Johnsson, et al.
American Journal of Human Genetics|March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisisS Saunier, J Calado, F Benessy, et al.
Genomics|October 10, 1995
Physical mapping of the human ELA1 gene between D12S361 and D12S347 on chromosome 12q13R L Davies, S J Yoon, J Weissenbach, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|March 1, 1995
Establishment of the marker order pter-NRAS-NGFB-D1S189-D1S252-D1S440-D1S453-D1S514-CEN-D1S442-D1S498-qte r in relation to the centromere on human chromosome 1N Hoggard, B Brintnell, Y Hey, et al.
Human Molecular Genetics|August 1, 1995
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneityL Parmentier, C Blanchet-Bardon, S Nguyen, et al.
American Journal of Human Genetics|October 1, 1995
Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17pR Goliath, Y Shugart, P Janssens, et al.
Human Genetics|April 1, 1998
Linkage between atopy and the IgE high-affinity receptor gene at 11q13 in atopic dermatitis familiesR Fölster-Holst, H W Moises, L Yang, et al.
American Journal of Human Genetics|January 1, 1995
Refining the localization of the PKD2 locus on chromosome 4q by linkage analysis in Spanish families with autosomal dominant polycystic kidney disease type 2J L San Millán, M Viribay, B Peral, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
Pageof 37