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I A Glass

Showing results (31-40 of 42) with videos related to

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Journal of Medical Genetics|December 1, 1993
Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosomeI A Glass, P Good, M P Coleman, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|October 23, 2001
Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genesS C Healey, K M Kirk, V J Hyland, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophyA M Lehman, P Eydoux, D Doherty, et al.
Journal of Medical Genetics|October 4, 2002
Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhoodS F Flanagan, C F J Munns, M Hayes, et al.
American Journal of Human Genetics|March 1, 1991
Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeG K Suthers, J C Mulley, M A Voelckel, et al.
Genomics|July 1, 1991
Linkage homogeneity near the fragile X locus in normal and fragile X familiesG K Suthers, J C Mulley, M A Voelckel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Familial growth and skeletal features associated with SHOX haploinsufficiencyC F J Munns, I A Glass, S Flanagan, et al.
Journal of Medical Genetics|September 13, 2005
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.
American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.
Journal of Medical Genetics|July 4, 2009
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)D Doherty, M A Parisi, L S Finn, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|December 1, 1993
Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosomeI A Glass, P Good, M P Coleman, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|October 23, 2001
Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genesS C Healey, K M Kirk, V J Hyland, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophyA M Lehman, P Eydoux, D Doherty, et al.
Journal of Medical Genetics|October 4, 2002
Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhoodS F Flanagan, C F J Munns, M Hayes, et al.
American Journal of Human Genetics|March 1, 1991
Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeG K Suthers, J C Mulley, M A Voelckel, et al.
Genomics|July 1, 1991
Linkage homogeneity near the fragile X locus in normal and fragile X familiesG K Suthers, J C Mulley, M A Voelckel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Familial growth and skeletal features associated with SHOX haploinsufficiencyC F J Munns, I A Glass, S Flanagan, et al.
Journal of Medical Genetics|September 13, 2005
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.
American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.
Journal of Medical Genetics|July 4, 2009
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)D Doherty, M A Parisi, L S Finn, et al.
Pageof 5