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K W Gripp

Showing results (1-10 of 29) with videos related to

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Clinical Dysmorphology|October 1, 1996
Bilateral duplication of the primary ulnar ossification center in Ellis-van Creveld syndromeK W Gripp, C I Scott, L Nicholson
American Journal of Medical Genetics|February 2, 1996
Apparently new syndrome of congenital cataracts, sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardationK W Gripp, L Nicholson, C I Scott
Human Mutation|January 29, 2000
Mutations in the human TWIST geneK W Gripp, E H Zackai, C A Stolle
American Journal of Medical Genetics|May 8, 2000
Craniosynostosis: molecular testing-a necessity for counselingE H Zackai, K W Gripp, C A Stolle
American Journal of Medical Genetics|March 17, 1999
Not Antley-Bixler syndromeK W Gripp, E H Zackai, M M Cohen
Clinical Genetics|February 1, 2017
Attenuated phenotype of Costello syndrome and early death in a patient with an HRAS mutation (c.179G>T; p.Gly60Val) affecting signalling dynamicsK W Gripp, V Kolbe, L I Brandenstein, et al.
American Journal of Medical Genetics|March 4, 2000
Second case of bladder carcinoma in a patient with Costello syndromeK W Gripp, C I Scott, L Nicholson, et al.
Skeletal Radiology|February 1, 1997
Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tardaK W Gripp, C I Scott, L Nicholson, et al.
American Journal of Medical Genetics|November 11, 1996
Extending the spectrum of distal arthrogryposisK W Gripp, C I Scott, B C Brockett, et al.
Clinical Genetics|March 16, 2017
Constitutional LZTR1 mutation presenting with a unilateral vestibular schwannoma in a teenagerK W Gripp, L Baker, V Kandula, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Clinical Dysmorphology|October 1, 1996
Bilateral duplication of the primary ulnar ossification center in Ellis-van Creveld syndromeK W Gripp, C I Scott, L Nicholson
American Journal of Medical Genetics|February 2, 1996
Apparently new syndrome of congenital cataracts, sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardationK W Gripp, L Nicholson, C I Scott
Human Mutation|January 29, 2000
Mutations in the human TWIST geneK W Gripp, E H Zackai, C A Stolle
American Journal of Medical Genetics|May 8, 2000
Craniosynostosis: molecular testing-a necessity for counselingE H Zackai, K W Gripp, C A Stolle
American Journal of Medical Genetics|March 17, 1999
Not Antley-Bixler syndromeK W Gripp, E H Zackai, M M Cohen
Clinical Genetics|February 1, 2017
Attenuated phenotype of Costello syndrome and early death in a patient with an HRAS mutation (c.179G>T; p.Gly60Val) affecting signalling dynamicsK W Gripp, V Kolbe, L I Brandenstein, et al.
American Journal of Medical Genetics|March 4, 2000
Second case of bladder carcinoma in a patient with Costello syndromeK W Gripp, C I Scott, L Nicholson, et al.
Skeletal Radiology|February 1, 1997
Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tardaK W Gripp, C I Scott, L Nicholson, et al.
American Journal of Medical Genetics|November 11, 1996
Extending the spectrum of distal arthrogryposisK W Gripp, C I Scott, B C Brockett, et al.
Clinical Genetics|March 16, 2017
Constitutional LZTR1 mutation presenting with a unilateral vestibular schwannoma in a teenagerK W Gripp, L Baker, V Kandula, et al.
Pageof 3