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Showing results (91-100 of 120) with videos related to

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American Journal of Human Genetics|June 12, 1999
Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasiaP Holden, E G Canty, G R Mortier, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
Journal of Medical Genetics|June 1, 1996
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasiaG A Wallis, B Rash, B Sykes, et al.
Genomics|July 1, 1991
A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locusL M Davis, B Zabel, G Senger, et al.
American Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.
Human Molecular Genetics|April 18, 2000
LMX1B transactivation and expression in nail-patella syndromeS D Dreyer, R Morello, M S German, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clonesL M Davis, G Senger, H J Lüdecke, et al.
Cancer Research|June 12, 1999
RetractionR F Schwerdtle, C Neuhaus, E Weidt, et al.
American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.
American Journal of Human Genetics|October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasiaW A Sweetman, B Rash, B Sykes, et al.
Pageof 12

Showing results (91-100 of 120) with videos related to

Sort By:
Pageof 12
American Journal of Human Genetics|June 12, 1999
Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasiaP Holden, E G Canty, G R Mortier, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
Journal of Medical Genetics|June 1, 1996
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasiaG A Wallis, B Rash, B Sykes, et al.
Genomics|July 1, 1991
A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locusL M Davis, B Zabel, G Senger, et al.
American Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.
Human Molecular Genetics|April 18, 2000
LMX1B transactivation and expression in nail-patella syndromeS D Dreyer, R Morello, M S German, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clonesL M Davis, G Senger, H J Lüdecke, et al.
Cancer Research|June 12, 1999
RetractionR F Schwerdtle, C Neuhaus, E Weidt, et al.
American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.
American Journal of Human Genetics|October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasiaW A Sweetman, B Rash, B Sykes, et al.
Pageof 12