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R E Stevenson

Showing results (61-70 of 126) with videos related to

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Lancet (London, England)|May 6, 1972
Allelism, non-allelism, and genetic compounds among the mucopolysaccharidosesV A McKusick, R R Howell, I E Hussels, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.
Clinical Genetics|April 10, 2002
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.
American Journal of Medical Genetics|June 1, 1994
Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8qY Wang, K Treat, R J Schroer, et al.
Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.
The American Journal of Clinical Nutrition|October 1, 1995
Folic acid absorption in women with a history of pregnancy with neural tube defectB A Davis, L B Bailey, J F Gregory, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2012
Short-term memory deficits in carrier females with KDM5C mutationsR J Simensen, R C Rogers, J S Collins, et al.
Pediatrics|October 1, 1983
Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile typeR E Stevenson, M Lubinsky, H A Taylor, et al.
Journal of Medical Genetics|June 3, 2006
Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 geneH Lubs, F E Abidi, R Echeverri, et al.
Clinical Genetics|October 1, 1996
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21B Häne, R J Schroer, J F Arena, et al.
Pageof 13

Showing results (61-70 of 126) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|May 6, 1972
Allelism, non-allelism, and genetic compounds among the mucopolysaccharidosesV A McKusick, R R Howell, I E Hussels, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.
Clinical Genetics|April 10, 2002
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.
American Journal of Medical Genetics|June 1, 1994
Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8qY Wang, K Treat, R J Schroer, et al.
Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.
The American Journal of Clinical Nutrition|October 1, 1995
Folic acid absorption in women with a history of pregnancy with neural tube defectB A Davis, L B Bailey, J F Gregory, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2012
Short-term memory deficits in carrier females with KDM5C mutationsR J Simensen, R C Rogers, J S Collins, et al.
Pediatrics|October 1, 1983
Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile typeR E Stevenson, M Lubinsky, H A Taylor, et al.
Journal of Medical Genetics|June 3, 2006
Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 geneH Lubs, F E Abidi, R Echeverri, et al.
Clinical Genetics|October 1, 1996
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21B Häne, R J Schroer, J F Arena, et al.
Pageof 13