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P Monaco

Showing results (611-620 of 719) with videos related to

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European Journal of Human Genetics : EJHG|March 14, 2000
Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostosesC Dobson-Stone, R D Cox, L Lonie, et al.
Human Molecular Genetics|April 1, 1995
Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22A P Miller, K Gustashaw, D J Wolff, et al.
Transplantation|January 15, 1995
Effect of early administration of donor bone marrow cells on renal allograft survival in dogs treated with antilymphocyte serum and cyclosporineW C Hartner, T G Markees, S R De Fazio, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairmentDianne F Newbury, Pamela C Warburton, Natalie Wilson, et al.
European Journal of Human Genetics : EJHG|April 23, 2009
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collectionNuala H Sykes, Claudio Toma, Natalie Wilson, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|September 24, 2005
Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic lociJ Gayán, E G Willcutt, S E Fisher, et al.
Epilepsia|August 3, 2005
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosisAbdullah Al-Asmi, An C Jansen, AmanPreet Badhwar, et al.
Genomics|August 1, 1992
Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6L M Brzustowicz, P W Kleyn, F M Boyce, et al.
Journal of Neurodevelopmental Disorders|April 13, 2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autismVeronica J Vieland, Joachim Hallmayer, Yungui Huang, et al.
Nature|August 4, 1985
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segmentA P Monaco, C J Bertelson, W Middlesworth, et al.
Pageof 72

Showing results (611-620 of 719) with videos related to

Sort By:
Pageof 72
European Journal of Human Genetics : EJHG|March 14, 2000
Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostosesC Dobson-Stone, R D Cox, L Lonie, et al.
Human Molecular Genetics|April 1, 1995
Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22A P Miller, K Gustashaw, D J Wolff, et al.
Transplantation|January 15, 1995
Effect of early administration of donor bone marrow cells on renal allograft survival in dogs treated with antilymphocyte serum and cyclosporineW C Hartner, T G Markees, S R De Fazio, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairmentDianne F Newbury, Pamela C Warburton, Natalie Wilson, et al.
European Journal of Human Genetics : EJHG|April 23, 2009
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collectionNuala H Sykes, Claudio Toma, Natalie Wilson, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|September 24, 2005
Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic lociJ Gayán, E G Willcutt, S E Fisher, et al.
Epilepsia|August 3, 2005
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosisAbdullah Al-Asmi, An C Jansen, AmanPreet Badhwar, et al.
Genomics|August 1, 1992
Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6L M Brzustowicz, P W Kleyn, F M Boyce, et al.
Journal of Neurodevelopmental Disorders|April 13, 2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autismVeronica J Vieland, Joachim Hallmayer, Yungui Huang, et al.
Nature|August 4, 1985
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segmentA P Monaco, C J Bertelson, W Middlesworth, et al.
Pageof 72