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M Muenke

Showing results (31-40 of 104) with videos related to

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Cytogenetic and Genome Research|November 20, 2002
The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephalyJ D Karkera, S Izraeli, E Roessler, et al.
American Journal of Medical Genetics|October 23, 1997
Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromesK Yoshiura, N J Leysens, J Chang, et al.
Genomics|October 1, 1990
Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresisR E Schnur, R G Knowlton, M A Musarella, et al.
The Journal of Bone and Joint Surgery. American Volume|August 1, 1993
Genetic transmission of fibrodysplasia ossificans progressiva. Report of a familyF S Kaplan, W McCluskey, G Hahn, et al.
American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 18p11.3J Overhauser, H F Mitchell, E H Zackai, et al.
American Journal of Medical Genetics|July 27, 2001
SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literatureL Nanni, J E Ming, Y Du, et al.
Cancer Genetics and Cytogenetics|August 1, 1994
Loss of chromosome 8p sequences in human breast carcinoma cell linesM J Pykett, M E Murphy, P R Harnish, et al.
Human Molecular Genetics|September 25, 1997
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Human Genetics|January 27, 2000
Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8H J Lüdecke, O Schmidt, J Nardmann, et al.
American Journal of Medical Genetics|October 16, 1996
Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephalyJ R Sawyer, J L Lukacs, S J Hassed, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Cytogenetic and Genome Research|November 20, 2002
The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephalyJ D Karkera, S Izraeli, E Roessler, et al.
American Journal of Medical Genetics|October 23, 1997
Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromesK Yoshiura, N J Leysens, J Chang, et al.
Genomics|October 1, 1990
Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresisR E Schnur, R G Knowlton, M A Musarella, et al.
The Journal of Bone and Joint Surgery. American Volume|August 1, 1993
Genetic transmission of fibrodysplasia ossificans progressiva. Report of a familyF S Kaplan, W McCluskey, G Hahn, et al.
American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 18p11.3J Overhauser, H F Mitchell, E H Zackai, et al.
American Journal of Medical Genetics|July 27, 2001
SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literatureL Nanni, J E Ming, Y Du, et al.
Cancer Genetics and Cytogenetics|August 1, 1994
Loss of chromosome 8p sequences in human breast carcinoma cell linesM J Pykett, M E Murphy, P R Harnish, et al.
Human Molecular Genetics|September 25, 1997
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Human Genetics|January 27, 2000
Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8H J Lüdecke, O Schmidt, J Nardmann, et al.
American Journal of Medical Genetics|October 16, 1996
Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephalyJ R Sawyer, J L Lukacs, S J Hassed, et al.
Pageof 11