J E Ming|M Muenke - JoVE Visualize

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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.

Genomics|September 15, 1994

Structure of the human gene encoding the associated microfibrillar protein (MFAP1) and localization to chromosome 15q15-q21H Yeh, M Chow, W R Abrams, et al.

Translational Psychiatry|July 27, 2012

A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcomeM T Acosta, J I Vélez, M L Bustamante, et al.

Cellular Immunology|October 15, 1990

Distinctive features in the production of IL-6 by human T cellsJ E Ming, A Granelli-Piperno

Human Molecular Genetics|November 11, 1999

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephalyL Nanni, J E Ming, M Bocian, et al.

Nature Genetics|November 1, 1996

Mutations in the human Sonic Hedgehog gene cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.

Nature Genetics|October 1, 1996

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesG A Bellus, K Gaudenz, E H Zackai, et al.

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Showing results (31-40 of 112) with videos related to

Sort By:

Pageof 12

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.

Genomics|September 15, 1994

Structure of the human gene encoding the associated microfibrillar protein (MFAP1) and localization to chromosome 15q15-q21H Yeh, M Chow, W R Abrams, et al.

Translational Psychiatry|July 27, 2012

A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcomeM T Acosta, J I Vélez, M L Bustamante, et al.

Cellular Immunology|October 15, 1990

Distinctive features in the production of IL-6 by human T cellsJ E Ming, A Granelli-Piperno

Human Molecular Genetics|November 11, 1999

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephalyL Nanni, J E Ming, M Bocian, et al.

Nature Genetics|November 1, 1996

Mutations in the human Sonic Hedgehog gene cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.

Nature Genetics|October 1, 1996

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesG A Bellus, K Gaudenz, E H Zackai, et al.

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