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Human genetics

Showing results (1031-1040 of 9,569) with videos related to

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Human Genetics|January 28, 1976
Possible genetic consequences of relaxed selection against common disorders with complex inheritanceE Matsunaga
Human Genetics|January 28, 1976
[A case of testicular feminization with the karyotype 47, XXY (author's transl)]M Bartsch-Sandhoff, L Stephan, G Röhrborn, et al.
Human Genetics|February 29, 1976
Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20C G Palmer, C Poland, T Reed, et al.
Human Genetics|February 29, 1976
Dosage effect of SOD-A gene in 21-trisomic cellsN Crosti, A Serra, A Rigo, et al.
Human Genetics|September 19, 2003
NF1 exon 7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis 1 patientPatrizia Colapietro, Cristina Gervasini, Federica Natacci, et al.
Human Genetics|May 1, 1992
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 betaG de Saint Basile, L D Notarangelo, C Bonaiti-Pellié, et al.
Human Genetics|May 1, 1992
The human fumarylacetoacetase gene: characterisation of restriction fragment length polymorphisms and identification of haplotypes in tyrosinemia type 1 and pseudodeficiencyH Rootwelt, E A Kvittingen, K Høie, et al.
Human Genetics|July 1, 1992
Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxiaM Colombi, R Gardella, N Zoppi, et al.
Human Genetics|July 1, 1992
Reduced recombination and paternal age effect in Klinefelter syndromeI Lorda-Sanchez, F Binkert, M Maechler, et al.
Human Genetics|July 1, 1992
Three DNA markers for hypophosphataemic ricketsP S Rowe, A P Read, R Mountford, et al.
Pageof 957

Showing results (1031-1040 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|January 28, 1976
Possible genetic consequences of relaxed selection against common disorders with complex inheritanceE Matsunaga
Human Genetics|January 28, 1976
[A case of testicular feminization with the karyotype 47, XXY (author's transl)]M Bartsch-Sandhoff, L Stephan, G Röhrborn, et al.
Human Genetics|February 29, 1976
Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20C G Palmer, C Poland, T Reed, et al.
Human Genetics|February 29, 1976
Dosage effect of SOD-A gene in 21-trisomic cellsN Crosti, A Serra, A Rigo, et al.
Human Genetics|September 19, 2003
NF1 exon 7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis 1 patientPatrizia Colapietro, Cristina Gervasini, Federica Natacci, et al.
Human Genetics|May 1, 1992
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 betaG de Saint Basile, L D Notarangelo, C Bonaiti-Pellié, et al.
Human Genetics|May 1, 1992
The human fumarylacetoacetase gene: characterisation of restriction fragment length polymorphisms and identification of haplotypes in tyrosinemia type 1 and pseudodeficiencyH Rootwelt, E A Kvittingen, K Høie, et al.
Human Genetics|July 1, 1992
Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxiaM Colombi, R Gardella, N Zoppi, et al.
Human Genetics|July 1, 1992
Reduced recombination and paternal age effect in Klinefelter syndromeI Lorda-Sanchez, F Binkert, M Maechler, et al.
Human Genetics|July 1, 1992
Three DNA markers for hypophosphataemic ricketsP S Rowe, A P Read, R Mountford, et al.
Pageof 957