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M Muenke

Showing results (41-50 of 104) with videos related to

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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.
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.
Molecular Syndromology|November 1, 2012
High Intellectual Function in Individuals with Mutation-Positive Microform HoloprosencephalyB D Solomon, D E Pineda-Alvarez, A L Gropman, et al.
Genetics|October 19, 2001
Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1R M Clark, P C Marker, E Roessler, et al.
Clinical Genetics|November 29, 2016
Bi-allelic IARS mutations in a child with intra-uterine growth retardation, neonatal cholestasis, and mild developmental delayN Orenstein, K Weiss, S N Oprescu, et al.
The New England Journal of Medicine|August 22, 1996
Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressivaA B Shafritz, E M Shore, F H Gannon, et al.
Prenatal Diagnosis|December 18, 2001
Semilobar holoprosencephaly in a 46,XY female fetusI Witters, P Moerman, M Muenke, et al.
Molecular Syndromology|November 4, 2010
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in HumansR F Arauz, B D Solomon, D E Pineda-Alvarez, et al.
Pageof 11

Showing results (41-50 of 104) with videos related to

Sort By:
Pageof 11
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.
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.
Molecular Syndromology|November 1, 2012
High Intellectual Function in Individuals with Mutation-Positive Microform HoloprosencephalyB D Solomon, D E Pineda-Alvarez, A L Gropman, et al.
Genetics|October 19, 2001
Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1R M Clark, P C Marker, E Roessler, et al.
Clinical Genetics|November 29, 2016
Bi-allelic IARS mutations in a child with intra-uterine growth retardation, neonatal cholestasis, and mild developmental delayN Orenstein, K Weiss, S N Oprescu, et al.
The New England Journal of Medicine|August 22, 1996
Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressivaA B Shafritz, E M Shore, F H Gannon, et al.
Prenatal Diagnosis|December 18, 2001
Semilobar holoprosencephaly in a 46,XY female fetusI Witters, P Moerman, M Muenke, et al.
Molecular Syndromology|November 4, 2010
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in HumansR F Arauz, B D Solomon, D E Pineda-Alvarez, et al.
Pageof 11