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N J Carpenter

Showing results (31-40 of 59) with videos related to

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Clinical Pediatrics|December 1, 1982
A condition resembling congenital hypoplastic anemia occurring in a mother and sonG McFarland, B Say, N J Carpenter, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2N J Carpenter, W T Brown, Y Qu, et al.
American Journal of Medical Genetics|April 1, 1992
Linkage and risk assessment in fragile X families using new DNA probes at Xq27N J Carpenter, J Swartz-Boyd, J K Prichard, et al.
Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.
American Journal of Medical Genetics|July 9, 1999
Refined gene localization for the Miles-Carpenter syndrome (MCS)D Tackels, C E Schwartz, N J Carpenter, et al.
Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.
Annales De Genetique|January 1, 1996
Familial deletion of chromosome 18 (p11.2)G V Velagaleti, S Harris, N J Carpenter, et al.
The Journal of the Oklahoma State Medical Association|November 1, 1996
Charcot-Marie-Tooth disease type 1A: a family study with microsatellitesY Qu, N J Carpenter, L Whetsell, et al.
American Journal of Medical Genetics|July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridizationV V Rao, N J Carpenter, M Gucsavas, et al.
American Journal of Human Genetics|May 23, 1998
Diversity of cystic fibrosis mutation-screening practicesW W Grody, R J Desnick, N J Carpenter, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Clinical Pediatrics|December 1, 1982
A condition resembling congenital hypoplastic anemia occurring in a mother and sonG McFarland, B Say, N J Carpenter, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2N J Carpenter, W T Brown, Y Qu, et al.
American Journal of Medical Genetics|April 1, 1992
Linkage and risk assessment in fragile X families using new DNA probes at Xq27N J Carpenter, J Swartz-Boyd, J K Prichard, et al.
Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.
American Journal of Medical Genetics|July 9, 1999
Refined gene localization for the Miles-Carpenter syndrome (MCS)D Tackels, C E Schwartz, N J Carpenter, et al.
Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.
Annales De Genetique|January 1, 1996
Familial deletion of chromosome 18 (p11.2)G V Velagaleti, S Harris, N J Carpenter, et al.
The Journal of the Oklahoma State Medical Association|November 1, 1996
Charcot-Marie-Tooth disease type 1A: a family study with microsatellitesY Qu, N J Carpenter, L Whetsell, et al.
American Journal of Medical Genetics|July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridizationV V Rao, N J Carpenter, M Gucsavas, et al.
American Journal of Human Genetics|May 23, 1998
Diversity of cystic fibrosis mutation-screening practicesW W Grody, R J Desnick, N J Carpenter, et al.
Pageof 6