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K W Gripp

Showing results (11-20 of 29) with videos related to

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American Journal of Human Genetics|March 11, 2000
Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding proteinA Hinek, A C Smith, E M Cutiongco, et al.
American Journal of Medical Genetics|March 9, 1999
Aphallia as part of urorectal septum malformation sequence in an infant of a diabetic motherK W Gripp, M Barr, G Anadiotis, et al.
American Journal of Medical Genetics|February 11, 1997
Diaphragmatic hernia-exomphalos-hypertelorism syndrome: a new case and further evidence of autosomal recessive inheritanceK W Gripp, D Donnai, C L Clericuzio, et al.
American Journal of Medical Genetics|February 6, 1999
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndromeK W Gripp, C A Stolle, L Celle, et al.
American Journal of Medical Genetics|March 31, 1997
Nasal dimple as part of the 22q11.2 deletion syndromeK W Gripp, D M McDonald-McGinn, D A Driscoll, et al.
Plastic and Reconstructive Surgery|December 18, 2001
Clinical characteristics of patients with unicoronal synostosis and mutations of fibroblast growth factor receptor 3: a preliminary reportL B Cassileth, S P Bartlett, P M Glat, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Chromosomal mapping of the genes GPRK5 and GPRK6 encoding G protein-coupled receptor kinases GRK5 and GRK6F Bullrich, T Druck, P Kunapuli, et al.
American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.
Nature Genetics|June 3, 2000
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determinationK W Gripp, D Wotton, M C Edwards, et al.
American Journal of Medical Genetics|June 26, 2001
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemiaK W Gripp, D M McDonald-McGinn, D La Rossa, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|March 11, 2000
Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding proteinA Hinek, A C Smith, E M Cutiongco, et al.
American Journal of Medical Genetics|March 9, 1999
Aphallia as part of urorectal septum malformation sequence in an infant of a diabetic motherK W Gripp, M Barr, G Anadiotis, et al.
American Journal of Medical Genetics|February 11, 1997
Diaphragmatic hernia-exomphalos-hypertelorism syndrome: a new case and further evidence of autosomal recessive inheritanceK W Gripp, D Donnai, C L Clericuzio, et al.
American Journal of Medical Genetics|February 6, 1999
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndromeK W Gripp, C A Stolle, L Celle, et al.
American Journal of Medical Genetics|March 31, 1997
Nasal dimple as part of the 22q11.2 deletion syndromeK W Gripp, D M McDonald-McGinn, D A Driscoll, et al.
Plastic and Reconstructive Surgery|December 18, 2001
Clinical characteristics of patients with unicoronal synostosis and mutations of fibroblast growth factor receptor 3: a preliminary reportL B Cassileth, S P Bartlett, P M Glat, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Chromosomal mapping of the genes GPRK5 and GPRK6 encoding G protein-coupled receptor kinases GRK5 and GRK6F Bullrich, T Druck, P Kunapuli, et al.
American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.
Nature Genetics|June 3, 2000
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determinationK W Gripp, D Wotton, M C Edwards, et al.
American Journal of Medical Genetics|June 26, 2001
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemiaK W Gripp, D M McDonald-McGinn, D La Rossa, et al.
Pageof 3