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I A Glass

Showing results (21-30 of 42) with videos related to

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American Journal of Medical Genetics|February 1, 1991
Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markersI A Glass, L A Pirrit, E M White, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiencyC F J Munns, M Berry, D Vickers, et al.
American Journal of Medical Genetics|June 26, 2001
Premature calvarial synostosis and epidermal hyperplasia (Beare-Stevenson syndrome-like anomalies) resulting from a P250R missense mutation in the gene encoding fibroblast growth factor receptor 3T Roscioli, S Flanagan, R J Mortimore, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 17, 2003
Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangementsV L Souter, I A Glass, D B Chapman, et al.
Journal of Medical Genetics|August 1, 1992
Investigation of a female manifesting Becker muscular dystrophyI A Glass, L V Nicholson, E Watkiss, et al.
American Journal of Medical Genetics|August 1, 1992
Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experienceI A Glass, R G Del Mastro, W G Lanyon, et al.
Lancet (London, England)|April 12, 1997
Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosisD M Moloney, S A Wall, G J Ashworth, et al.
The Journal of Clinical Endocrinology and Metabolism|August 5, 2004
Expression of SHOX in human fetal and childhood growth plateC J F Munns, H R Haase, L M Crowther, et al.
American Journal of Medical Genetics|September 24, 1999
Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: evidence for an ancestral founder of the common G111R mutationA De Siervi, M V Rossetti, V E Parera, et al.
Hand Surgery : an International Journal Devoted to Hand and Upper Limb Surgery and Related Research : Journal of the Asia-Pacific Federation of Societies for Surgery of the Hand|October 26, 2001
Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plateC F Munns, I A Glass, R LaBrom, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|February 1, 1991
Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markersI A Glass, L A Pirrit, E M White, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiencyC F J Munns, M Berry, D Vickers, et al.
American Journal of Medical Genetics|June 26, 2001
Premature calvarial synostosis and epidermal hyperplasia (Beare-Stevenson syndrome-like anomalies) resulting from a P250R missense mutation in the gene encoding fibroblast growth factor receptor 3T Roscioli, S Flanagan, R J Mortimore, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 17, 2003
Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangementsV L Souter, I A Glass, D B Chapman, et al.
Journal of Medical Genetics|August 1, 1992
Investigation of a female manifesting Becker muscular dystrophyI A Glass, L V Nicholson, E Watkiss, et al.
American Journal of Medical Genetics|August 1, 1992
Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experienceI A Glass, R G Del Mastro, W G Lanyon, et al.
Lancet (London, England)|April 12, 1997
Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosisD M Moloney, S A Wall, G J Ashworth, et al.
The Journal of Clinical Endocrinology and Metabolism|August 5, 2004
Expression of SHOX in human fetal and childhood growth plateC J F Munns, H R Haase, L M Crowther, et al.
American Journal of Medical Genetics|September 24, 1999
Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: evidence for an ancestral founder of the common G111R mutationA De Siervi, M V Rossetti, V E Parera, et al.
Hand Surgery : an International Journal Devoted to Hand and Upper Limb Surgery and Related Research : Journal of the Asia-Pacific Federation of Societies for Surgery of the Hand|October 26, 2001
Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plateC F Munns, I A Glass, R LaBrom, et al.
Pageof 5