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R E Stevenson

Showing results (51-60 of 126) with videos related to

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American Journal of Medical Genetics|February 1, 1992
Duplication of distal 19q: clinical report and reviewE Boyd, F S Grass, J C Parke, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1975
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblastsH A Taylor, G H Thomas, A Aylsworth, et al.
Clinical Genetics|May 29, 2002
Cognitive function in Coffin-Lowry syndromeR J Simensen, F Abidi, J S Collins, et al.
American Journal of Medical Genetics|October 26, 2000
Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndromeR E Stevenson, F Abidi, C E Schwartz, et al.
Pediatric Clinics of North America|April 11, 1992
Fellowships and career development in dysmorphology and clinical geneticsJ M Graham, C J Curry, H E Hoyme, et al.
Journal of the South Carolina Medical Association (1975)|September 1, 1982
Fragile X syndrome in South CarolinaR A Saul, R E Stevenson, R J Simensen, et al.
Transactions of the Association of American Physicians|January 1, 1972
Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapyV A McKusick, R R Howell, I E Hussels, et al.
American Journal of Human Genetics|September 1, 1990
Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21C E Schwartz, J Ulmer, A Brown, et al.
JAMA|September 27, 1976
Hepatic adenomata with type 1 glycogen storage diseaseR R Howell, R E Stevenson, Y Ben-Menachem, et al.
American Journal of Medical Genetics|July 1, 1983
Transport media for tissue specimens: a comparative studyW E Potts, R A Saul, S E Riley, et al.
Pageof 13

Showing results (51-60 of 126) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|February 1, 1992
Duplication of distal 19q: clinical report and reviewE Boyd, F S Grass, J C Parke, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1975
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblastsH A Taylor, G H Thomas, A Aylsworth, et al.
Clinical Genetics|May 29, 2002
Cognitive function in Coffin-Lowry syndromeR J Simensen, F Abidi, J S Collins, et al.
American Journal of Medical Genetics|October 26, 2000
Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndromeR E Stevenson, F Abidi, C E Schwartz, et al.
Pediatric Clinics of North America|April 11, 1992
Fellowships and career development in dysmorphology and clinical geneticsJ M Graham, C J Curry, H E Hoyme, et al.
Journal of the South Carolina Medical Association (1975)|September 1, 1982
Fragile X syndrome in South CarolinaR A Saul, R E Stevenson, R J Simensen, et al.
Transactions of the Association of American Physicians|January 1, 1972
Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapyV A McKusick, R R Howell, I E Hussels, et al.
American Journal of Human Genetics|September 1, 1990
Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21C E Schwartz, J Ulmer, A Brown, et al.
JAMA|September 27, 1976
Hepatic adenomata with type 1 glycogen storage diseaseR R Howell, R E Stevenson, Y Ben-Menachem, et al.
American Journal of Medical Genetics|July 1, 1983
Transport media for tissue specimens: a comparative studyW E Potts, R A Saul, S E Riley, et al.
Pageof 13