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H J Stalker

Showing results (11-20 of 16) with videos related to

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Human Mutation|January 1, 1997
NF1 mutation analysis using a combined heteroduplex/SSCP approachC R Abernathy, S A Rasmussen, H J Stalker, et al.
American Journal of Medical Genetics|September 6, 1996
Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?S A Rasmussen, C A Williams, E M Ayoub, et al.
Human Mutation|April 17, 1999
Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. OnlineS Krkljus, C R Abernathy, J S Johnson, et al.
American Journal of Medical Genetics|April 29, 1998
Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiencyR T Zori, F Z Boyar, W N Williams, et al.
Clinical Genetics|February 16, 2002
A family with a grand-maternally derived interstitial duplication of proximal 15qF Z Boyar, M M Whitney, A C Lossie, et al.
Genomics|May 20, 1999
Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23S A Boyadjiev, E W Jabs, M LaBuda, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Human Mutation|January 1, 1997
NF1 mutation analysis using a combined heteroduplex/SSCP approachC R Abernathy, S A Rasmussen, H J Stalker, et al.
American Journal of Medical Genetics|September 6, 1996
Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?S A Rasmussen, C A Williams, E M Ayoub, et al.
Human Mutation|April 17, 1999
Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. OnlineS Krkljus, C R Abernathy, J S Johnson, et al.
American Journal of Medical Genetics|April 29, 1998
Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiencyR T Zori, F Z Boyar, W N Williams, et al.
Clinical Genetics|February 16, 2002
A family with a grand-maternally derived interstitial duplication of proximal 15qF Z Boyar, M M Whitney, A C Lossie, et al.
Genomics|May 20, 1999
Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23S A Boyadjiev, E W Jabs, M LaBuda, et al.
Pageof 2