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B R DuPont

Showing results (21-30 of 29) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1996
Assignment of matrix metalloproteinase 9 (Mmp9) to mouse chromosome 2 bands H1-H2B R DuPont, R Linn, C B Knight, et al.
American Journal of Medical Genetics|April 29, 1998
Chromosome 18q paracentric inversion in a family with mental retardation and hearing lossK M Keppler-Noreuil, A J Carroll, S C Finley, et al.
Cytogenetic and Genome Research|November 9, 2005
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomaliesS S Bhat, K R Schmidt, S Ladd, et al.
Clinical Genetics|November 17, 2007
Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autismS S Bhat, S Ladd, F Grass, et al.
Journal of Dental Research|June 1, 2000
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth developmentC C Hu, T C Hart, B R Dupont, et al.
American Journal of Medical Genetics|July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18qJ D Cody, P D Ghidoni, B R DuPont, et al.
American Journal of Medical Genetics|July 25, 1997
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiencyC T Gay, L J Hardies, R A Rauch, et al.
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of matrix metalloproteinase 9 (Mmp9) to mouse chromosome 2 bands H1-H2B R DuPont, R Linn, C B Knight, et al.
American Journal of Medical Genetics|April 29, 1998
Chromosome 18q paracentric inversion in a family with mental retardation and hearing lossK M Keppler-Noreuil, A J Carroll, S C Finley, et al.
Cytogenetic and Genome Research|November 9, 2005
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomaliesS S Bhat, K R Schmidt, S Ladd, et al.
Clinical Genetics|November 17, 2007
Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autismS S Bhat, S Ladd, F Grass, et al.
Journal of Dental Research|June 1, 2000
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth developmentC C Hu, T C Hart, B R Dupont, et al.
American Journal of Medical Genetics|July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18qJ D Cody, P D Ghidoni, B R DuPont, et al.
American Journal of Medical Genetics|July 25, 1997
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiencyC T Gay, L J Hardies, R A Rauch, et al.
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
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