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D Abuelo

Showing results (1-10 of 16) with videos related to

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Dermatologic Clinics|January 1, 1987
Genetic principlesD Abuelo
Clinical Genetics|May 1, 1988
Counseling needs and attitudes toward prenatal diagnosis and abortion in fragile-X familiesD L Meryash, D Abuelo
American Journal of Perinatology|April 1, 1986
Midtrimester diagnosis of severe deforming osteogenesis imperfecta with autosomal dominant inheritanceM W Carpenter, D Abuelo, C Neave
American Journal of Human Genetics|September 1, 1989
Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid proteinS Gencic, D Abuelo, M Ambler, et al.
Pediatric Pathology|May 1, 1994
Fryns syndrome: a new definitionH Pinar, M W Carpenter, D Abuelo, et al.
Journal of Medical Genetics|December 1, 1977
Partial trisomy 8 (trisomy 8q2106 leads to 8qter)D Abuelo, D P Perl, C Henkle, et al.
Clinical Genetics|August 1, 1985
Frequency of fragile X chromosome in normal femalesD Abuelo, K Castree, S Pueschel, et al.
American Journal of Medical Genetics|October 1, 1986
Risk for trisomy 21 in offspring of individuals who have relatives with trisomy 21D Abuelo, G Barsel-Bowers, W Busch, et al.
Journal of Lipid Research|April 1, 1995
Identification of 8-dehydrocholesterol (cholesta-5,8-dien-3 beta-ol) in patients with Smith-Lemli-Opitz syndromeA K Batta, G S Tint, S Shefer, et al.
Journal of Medical Genetics|May 1, 1988
Lethal osteogenesis imperfecta associated with 46,XY,inv(7)(p13q22) karyotypeA S Knisely, A Richardson, D Abuelo, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Dermatologic Clinics|January 1, 1987
Genetic principlesD Abuelo
Clinical Genetics|May 1, 1988
Counseling needs and attitudes toward prenatal diagnosis and abortion in fragile-X familiesD L Meryash, D Abuelo
American Journal of Perinatology|April 1, 1986
Midtrimester diagnosis of severe deforming osteogenesis imperfecta with autosomal dominant inheritanceM W Carpenter, D Abuelo, C Neave
American Journal of Human Genetics|September 1, 1989
Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid proteinS Gencic, D Abuelo, M Ambler, et al.
Pediatric Pathology|May 1, 1994
Fryns syndrome: a new definitionH Pinar, M W Carpenter, D Abuelo, et al.
Journal of Medical Genetics|December 1, 1977
Partial trisomy 8 (trisomy 8q2106 leads to 8qter)D Abuelo, D P Perl, C Henkle, et al.
Clinical Genetics|August 1, 1985
Frequency of fragile X chromosome in normal femalesD Abuelo, K Castree, S Pueschel, et al.
American Journal of Medical Genetics|October 1, 1986
Risk for trisomy 21 in offspring of individuals who have relatives with trisomy 21D Abuelo, G Barsel-Bowers, W Busch, et al.
Journal of Lipid Research|April 1, 1995
Identification of 8-dehydrocholesterol (cholesta-5,8-dien-3 beta-ol) in patients with Smith-Lemli-Opitz syndromeA K Batta, G S Tint, S Shefer, et al.
Journal of Medical Genetics|May 1, 1988
Lethal osteogenesis imperfecta associated with 46,XY,inv(7)(p13q22) karyotypeA S Knisely, A Richardson, D Abuelo, et al.
Pageof 2