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R C Michaelis

Showing results (31-40 of 44) with videos related to

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American Journal of Medical Genetics|July 13, 2001
Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autismS M Plank, S A Copeland-Yates, K Sossey-Alaoui, et al.
Prenatal Diagnosis|March 31, 2000
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprintingC C Glenn, G Deng, R C Michaelis, et al.
American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.
American Journal of Medical Genetics|May 5, 2001
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocationL L Bassett, R C Michaelis, M H Geiger, et al.
American Journal of Medical Genetics|March 21, 1998
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11BR C Michaelis, G V Velagaleti, C Jones, et al.
Journal of Medical Genetics|October 10, 1997
The elusive Angelman syndrome critical regionR J Trent, L J Sheffield, Z M Deng, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Chromosome duplications and deletions and their mechanisms of originA T Tharapel, R C Michaelis, G V Velagaleti, et al.
Journal of Autism and Developmental Disorders|October 20, 2000
The HOPA gene dodecamer duplication is not a significant etiological factor in autismR C Michaelis, S A Copeland-Yates, K Sossey-Alaoui, et al.
American Journal of Medical Genetics|April 17, 1998
Autism and maternally derived aberrations of chromosome 15qR J Schroer, M C Phelan, R C Michaelis, et al.
Journal of Medical Genetics|November 25, 2003
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial caseJ Kohlhase, M Liebers, J Backe, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|July 13, 2001
Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autismS M Plank, S A Copeland-Yates, K Sossey-Alaoui, et al.
Prenatal Diagnosis|March 31, 2000
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprintingC C Glenn, G Deng, R C Michaelis, et al.
American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.
American Journal of Medical Genetics|May 5, 2001
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocationL L Bassett, R C Michaelis, M H Geiger, et al.
American Journal of Medical Genetics|March 21, 1998
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11BR C Michaelis, G V Velagaleti, C Jones, et al.
Journal of Medical Genetics|October 10, 1997
The elusive Angelman syndrome critical regionR J Trent, L J Sheffield, Z M Deng, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Chromosome duplications and deletions and their mechanisms of originA T Tharapel, R C Michaelis, G V Velagaleti, et al.
Journal of Autism and Developmental Disorders|October 20, 2000
The HOPA gene dodecamer duplication is not a significant etiological factor in autismR C Michaelis, S A Copeland-Yates, K Sossey-Alaoui, et al.
American Journal of Medical Genetics|April 17, 1998
Autism and maternally derived aberrations of chromosome 15qR J Schroer, M C Phelan, R C Michaelis, et al.
Journal of Medical Genetics|November 25, 2003
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial caseJ Kohlhase, M Liebers, J Backe, et al.
Pageof 5