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J M Gastier

Showing results (1-10 of 15) with videos related to

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Human Mutation|August 14, 1999
Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypesV Lemahieu, J M Gastier, U Francke
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2001
Evolutionary relationships among Rel domains indicate functional diversification by recombinationI A Graef, J M Gastier, U Francke, et al.
Human Mutation|October 3, 2000
Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndromeJ M Gastier, M A Berg, P Vesterhus, et al.
Genome Research|July 1, 1997
Characterization of Alu repeats that are associated with trinucleotide and tetranucleotide repeat microsatellitesC N Yandava, J M Gastier, J C Pulido, et al.
Clinical Genetics|April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technologyC E Cottrell, J Mendell, M Hart-Kothari, et al.
Genomics|July 1, 1995
Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehogV Marigo, D J Roberts, S M Lee, et al.
Human Molecular Genetics|October 1, 1995
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markersJ M Gastier, J C Pulido, S Sunden, et al.
Human Molecular Genetics|October 1, 1995
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage mapsV C Sheffield, J L Weber, K H Buetow, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 13, 2014
Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasiaJ K Trittmann, L D Nelin, E J Zmuda, et al.
American Journal of Medical Genetics|March 8, 2000
Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndromeP J Ferguson, S H Blanton, F T Saulsbury, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Mutation|August 14, 1999
Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypesV Lemahieu, J M Gastier, U Francke
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2001
Evolutionary relationships among Rel domains indicate functional diversification by recombinationI A Graef, J M Gastier, U Francke, et al.
Human Mutation|October 3, 2000
Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndromeJ M Gastier, M A Berg, P Vesterhus, et al.
Genome Research|July 1, 1997
Characterization of Alu repeats that are associated with trinucleotide and tetranucleotide repeat microsatellitesC N Yandava, J M Gastier, J C Pulido, et al.
Clinical Genetics|April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technologyC E Cottrell, J Mendell, M Hart-Kothari, et al.
Genomics|July 1, 1995
Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehogV Marigo, D J Roberts, S M Lee, et al.
Human Molecular Genetics|October 1, 1995
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markersJ M Gastier, J C Pulido, S Sunden, et al.
Human Molecular Genetics|October 1, 1995
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage mapsV C Sheffield, J L Weber, K H Buetow, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 13, 2014
Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasiaJ K Trittmann, L D Nelin, E J Zmuda, et al.
American Journal of Medical Genetics|March 8, 2000
Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndromeP J Ferguson, S H Blanton, F T Saulsbury, et al.
Pageof 2