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A Aylsworth

Showing results (1-10 of 11) with videos related to

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The Journal of the Florida Medical Association|September 1, 1970
Hunter-Hurler syndrome. A prototype for the study of storage diseaseR Julius, A Aylsworth, O Rennert
Clinical Genetics|April 1, 1985
Chromosomal abnormalities associated with congenital contractures (arthrogryposis)S D Reed, J G Hall, V M Riccardi, et al.
Neurology|January 1, 1971
Diagnostic techniques in metachromatic leukodystrophyR Julius, B Buehler, A Aylsworth, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Hypochondroplasia: molecular analysis of the fibroblast growth factor receptor 3 geneG A Bellus, I McIntosh, J Szabo, et al.
Human Molecular Genetics|August 1, 1995
Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHMM May, L Colleaux, A Murgia, 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.
Neuroendocrinology|April 1, 1982
Effects of morphine and naloxone on inhibition by ovarian hormones of pulsatile release of LH in ovariectomized ratsP W Sylvester, D A Van Vugt, C A Aylsworth, et al.
JAMA|July 2, 1997
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2D H Gutmann, A Aylsworth, J C Carey, et al.
Human Molecular Genetics|January 1, 1997
Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24A Gladwin, D Donnai, K Metcalfe, et al.
Nature Genetics|November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3M Gebbia, G B Ferrero, G Pilia, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The Journal of the Florida Medical Association|September 1, 1970
Hunter-Hurler syndrome. A prototype for the study of storage diseaseR Julius, A Aylsworth, O Rennert
Clinical Genetics|April 1, 1985
Chromosomal abnormalities associated with congenital contractures (arthrogryposis)S D Reed, J G Hall, V M Riccardi, et al.
Neurology|January 1, 1971
Diagnostic techniques in metachromatic leukodystrophyR Julius, B Buehler, A Aylsworth, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Hypochondroplasia: molecular analysis of the fibroblast growth factor receptor 3 geneG A Bellus, I McIntosh, J Szabo, et al.
Human Molecular Genetics|August 1, 1995
Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHMM May, L Colleaux, A Murgia, 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.
Neuroendocrinology|April 1, 1982
Effects of morphine and naloxone on inhibition by ovarian hormones of pulsatile release of LH in ovariectomized ratsP W Sylvester, D A Van Vugt, C A Aylsworth, et al.
JAMA|July 2, 1997
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2D H Gutmann, A Aylsworth, J C Carey, et al.
Human Molecular Genetics|January 1, 1997
Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24A Gladwin, D Donnai, K Metcalfe, et al.
Nature Genetics|November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3M Gebbia, G B Ferrero, G Pilia, et al.
Pageof 2