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S L Christian

Showing results (21-30 of 38) with videos related to

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The Journal of Pediatrics|January 8, 1999
Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitusS L Christian, B H Rich, C Loebl, et al.
Immunological Reviews|October 24, 2000
Targets of B-cell antigen receptor signaling: the phosphatidylinositol 3-kinase/Akt/glycogen synthase kinase-3 signaling pathway and the Rap1 GTPaseM R Gold, R J Ingham, S J McLeod, et al.
Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.
American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.
Journal of Medical Genetics|March 20, 2008
Disruption of contactin 4 in three subjects with autism spectrum disorderJ Roohi, C Montagna, D H Tegay, et al.
American Journal of Medical Genetics|September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndromeT Woodage, Z M Deng, M Prasad, et al.
Journal of Medical Genetics|December 1, 1998
Two 22q telomere deletions serendipitously detected by FISHK S Precht, C M Lese, R P Spiro, et al.
Journal of Medical Genetics|March 19, 2002
Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15qJ A Fantes, S K Mewborn, C M Lese, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Genome Research|March 21, 1998
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kbS L Christian, N K Bhatt, S A Martin, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
The Journal of Pediatrics|January 8, 1999
Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitusS L Christian, B H Rich, C Loebl, et al.
Immunological Reviews|October 24, 2000
Targets of B-cell antigen receptor signaling: the phosphatidylinositol 3-kinase/Akt/glycogen synthase kinase-3 signaling pathway and the Rap1 GTPaseM R Gold, R J Ingham, S J McLeod, et al.
Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.
American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.
Journal of Medical Genetics|March 20, 2008
Disruption of contactin 4 in three subjects with autism spectrum disorderJ Roohi, C Montagna, D H Tegay, et al.
American Journal of Medical Genetics|September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndromeT Woodage, Z M Deng, M Prasad, et al.
Journal of Medical Genetics|December 1, 1998
Two 22q telomere deletions serendipitously detected by FISHK S Precht, C M Lese, R P Spiro, et al.
Journal of Medical Genetics|March 19, 2002
Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15qJ A Fantes, S K Mewborn, C M Lese, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Genome Research|March 21, 1998
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kbS L Christian, N K Bhatt, S A Martin, et al.
Pageof 4