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M Muenke

Showing results (21-30 of 104) with videos related to

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Genomics|January 1, 1993
Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21A Köhler, C Logan, A L Joyner, et al.
Clinical Genetics|April 24, 2010
Submicroscopic familial chromosomal translocation between 7q and 12p mimicking an autosomal dominant holoprosencephaly syndromeK Izumi, D Culler, Bd Solomon, et al.
Molecular Genetics and Metabolism|July 31, 1998
Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4K Gaudenz, E Roessler, S Vainikka, et al.
Archives of Disease in Childhood|March 29, 2002
Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephalyH S Heussler, M Suri, I D Young, et al.
American Journal of Medical Genetics|March 10, 2000
Holoprosencephaly: molecular study of a California populationL Nanni, L A Croen, E J Lammer, et al.
Cytogenetics and Cell Genetics|January 1, 1995
A region-specific microdissection library for human chromosome 2p23-->p21 and the analysis of an interstitial deletion of 2p21F T Kao, J Yu, J Qi, et al.
American Journal of Medical Genetics|September 19, 1997
Clinical and molecular analysis in Joubert syndromeJ E Pellegrino, M W Lensch, M Muenke, et al.
Cytogenetics and Cell Genetics|August 31, 2000
The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephalyE Roessler, Y Du, A Glinka, et al.
American Journal of Medical Genetics|August 3, 2001
Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndromeL J Wong, T J Chen, P Dai, et al.
Genomics|January 1, 1996
Human enteric defensin genes: chromosomal map position and a model for possible evolutionary relationshipsC L Bevins, D E Jones, A Dutra, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Genomics|January 1, 1993
Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21A Köhler, C Logan, A L Joyner, et al.
Clinical Genetics|April 24, 2010
Submicroscopic familial chromosomal translocation between 7q and 12p mimicking an autosomal dominant holoprosencephaly syndromeK Izumi, D Culler, Bd Solomon, et al.
Molecular Genetics and Metabolism|July 31, 1998
Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4K Gaudenz, E Roessler, S Vainikka, et al.
Archives of Disease in Childhood|March 29, 2002
Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephalyH S Heussler, M Suri, I D Young, et al.
American Journal of Medical Genetics|March 10, 2000
Holoprosencephaly: molecular study of a California populationL Nanni, L A Croen, E J Lammer, et al.
Cytogenetics and Cell Genetics|January 1, 1995
A region-specific microdissection library for human chromosome 2p23-->p21 and the analysis of an interstitial deletion of 2p21F T Kao, J Yu, J Qi, et al.
American Journal of Medical Genetics|September 19, 1997
Clinical and molecular analysis in Joubert syndromeJ E Pellegrino, M W Lensch, M Muenke, et al.
Cytogenetics and Cell Genetics|August 31, 2000
The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephalyE Roessler, Y Du, A Glinka, et al.
American Journal of Medical Genetics|August 3, 2001
Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndromeL J Wong, T J Chen, P Dai, et al.
Genomics|January 1, 1996
Human enteric defensin genes: chromosomal map position and a model for possible evolutionary relationshipsC L Bevins, D E Jones, A Dutra, et al.
Pageof 11