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D A Pillers

Showing results (1-10 of 25) with videos related to

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Molecular Genetics and Metabolism|October 21, 1999
Dystrophin and the retinaD A Pillers
The New England Journal of Medicine|July 18, 1985
Familial IgA nephropathyD A Pillers, R D Koler
Hemoglobin|January 1, 1992
Hb Hope [beta 136(H14) Gly----Asp] and Hb E [beta 26(B8)Glu----Lys]: compound heterozygosity in a Thai Mien familyD A Pillers, M Jones, C Head, et al.
American Journal of Clinical Pathology|March 1, 1994
Misleading hepatitis C serology following administration of intravenous immunoglobulinR R Nixon, S A Smith, R L Johnson, et al.
American Journal of Medical Genetics|July 17, 1995
Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardationD M White, D A Pillers, J A Reiss, et al.
Biology of the Neonate|January 1, 1995
Furosemide pharmacokinetics following intratracheal instillation in the guinea pigS A Smith, D A Pillers, J T Gilhooly, et al.
Molecular Genetics and Metabolism|January 16, 1999
Redefinition of dystrophin isoform distribution in mouse tissue by RT-PCR implies role in nonmuscle manifestations of duchenne muscular dystrophyS A Tokarz, N M Duncan, S M Rash, et al.
Human Molecular Genetics|May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiologyV N D'Souza, T M Nguyen, G E Morris, et al.
The Laryngoscope|August 12, 1999
Normal cochlear function in mdx and mdx(Cv3) Duchenne muscular dystrophy mouse modelsD A Pillers, N M Duncan, S J Dwinnell, et al.
American Journal of Medical Genetics|May 1, 1990
Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasiaD A Pillers, R G Weleber, B R Powell, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|October 21, 1999
Dystrophin and the retinaD A Pillers
The New England Journal of Medicine|July 18, 1985
Familial IgA nephropathyD A Pillers, R D Koler
Hemoglobin|January 1, 1992
Hb Hope [beta 136(H14) Gly----Asp] and Hb E [beta 26(B8)Glu----Lys]: compound heterozygosity in a Thai Mien familyD A Pillers, M Jones, C Head, et al.
American Journal of Clinical Pathology|March 1, 1994
Misleading hepatitis C serology following administration of intravenous immunoglobulinR R Nixon, S A Smith, R L Johnson, et al.
American Journal of Medical Genetics|July 17, 1995
Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardationD M White, D A Pillers, J A Reiss, et al.
Biology of the Neonate|January 1, 1995
Furosemide pharmacokinetics following intratracheal instillation in the guinea pigS A Smith, D A Pillers, J T Gilhooly, et al.
Molecular Genetics and Metabolism|January 16, 1999
Redefinition of dystrophin isoform distribution in mouse tissue by RT-PCR implies role in nonmuscle manifestations of duchenne muscular dystrophyS A Tokarz, N M Duncan, S M Rash, et al.
Human Molecular Genetics|May 1, 1995
A novel dystrophin isoform is required for normal retinal electrophysiologyV N D'Souza, T M Nguyen, G E Morris, et al.
The Laryngoscope|August 12, 1999
Normal cochlear function in mdx and mdx(Cv3) Duchenne muscular dystrophy mouse modelsD A Pillers, N M Duncan, S J Dwinnell, et al.
American Journal of Medical Genetics|May 1, 1990
Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasiaD A Pillers, R G Weleber, B R Powell, et al.
Pageof 3