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de la CHAPELLE

Showing results (151-160 of 603) with videos related to

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Human Genetics|April 1, 1988
Characterization of a (Y;4) translocation by DNA hybridizationM Andersson, D C Page, L G Brown, et al.
Somatic Cell and Molecular Genetics|January 1, 1988
Demethylation of two specific DNA sequences in expressed human immunoglobulin light kappa constant genesN O Bianchi, P Peltomäki, M S Bianchi, et al.
Journal of Medical Genetics|February 1, 1996
The genetics of cornea plana congenitaE Tahvanainen, H Forsius, J Kolehmainen, et al.
The American Journal of Pathology|May 4, 2000
Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancersS A Kuismanen, M T Holmberg, R Salovaara, et al.
Anesthesia and Analgesia|May 29, 2002
The treatment of severe pulmonary edema induced by beta adrenergic agonist tocolytic therapy with continuous positive airway pressure delivered by face maskArnaud de La Chapelle, Stephane Benoit, Mohamed Bouregba, et al.
Biochimica Et Biophysica Acta|August 25, 1987
The pattern of methylation in rearranged and germ-line human immunoglobulin constant mu genesN O Bianchi, P Peltomäki, M S Bianchi, et al.
Journal of Medical Genetics|May 23, 1998
Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanismS Ala-Mello, E M Sankila, O Koskimies, et al.
Genomics|July 11, 1992
Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American familyA de la Chapelle, J Kere, G H Sack, et al.
Nature Genetics|November 1, 1992
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandJ Hästbacka, A de la Chapelle, I Kaitila, et al.
The New England Journal of Medicine|May 5, 1988
Clonal chromosomal abnormalities showing multiple-cell-lineage involvement in acute myeloid leukemiaM Keinänen, J D Griffin, C D Bloomfield, et al.
Pageof 61

Showing results (151-160 of 603) with videos related to

Sort By:
Pageof 61
Human Genetics|April 1, 1988
Characterization of a (Y;4) translocation by DNA hybridizationM Andersson, D C Page, L G Brown, et al.
Somatic Cell and Molecular Genetics|January 1, 1988
Demethylation of two specific DNA sequences in expressed human immunoglobulin light kappa constant genesN O Bianchi, P Peltomäki, M S Bianchi, et al.
Journal of Medical Genetics|February 1, 1996
The genetics of cornea plana congenitaE Tahvanainen, H Forsius, J Kolehmainen, et al.
The American Journal of Pathology|May 4, 2000
Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancersS A Kuismanen, M T Holmberg, R Salovaara, et al.
Anesthesia and Analgesia|May 29, 2002
The treatment of severe pulmonary edema induced by beta adrenergic agonist tocolytic therapy with continuous positive airway pressure delivered by face maskArnaud de La Chapelle, Stephane Benoit, Mohamed Bouregba, et al.
Biochimica Et Biophysica Acta|August 25, 1987
The pattern of methylation in rearranged and germ-line human immunoglobulin constant mu genesN O Bianchi, P Peltomäki, M S Bianchi, et al.
Journal of Medical Genetics|May 23, 1998
Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanismS Ala-Mello, E M Sankila, O Koskimies, et al.
Genomics|July 11, 1992
Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American familyA de la Chapelle, J Kere, G H Sack, et al.
Nature Genetics|November 1, 1992
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandJ Hästbacka, A de la Chapelle, I Kaitila, et al.
The New England Journal of Medicine|May 5, 1988
Clonal chromosomal abnormalities showing multiple-cell-lineage involvement in acute myeloid leukemiaM Keinänen, J D Griffin, C D Bloomfield, et al.
Pageof 61