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S F Slaney

Showing results (11-20 of 19) with videos related to

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Nature Genetics|May 1, 1996
Exclusive paternal origin of new mutations in Apert syndromeD M Moloney, S F Slaney, M Oldridge, et al.
Journal of Medical Genetics|September 1, 1994
Asymmetry and skin pigmentary anomalies in chromosome mosaicismC G Woods, A Bankier, J Curry, et al.
American Journal of Human Genetics|May 1, 1996
Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndromeS F Slaney, M Oldridge, J A Hurst, et al.
Nature Genetics|February 1, 1995
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypesP Rutland, L J Pulleyn, W Reardon, et al.
Archives of Disease in Childhood|January 1, 1995
DNA testing for fragile X syndrome in schools for learning difficultiesS F Slaney, A O Wilkie, M C Hirst, et al.
Nature Genetics|February 1, 1995
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndromeA O Wilkie, S F Slaney, M Oldridge, et al.
Human Molecular Genetics|June 1, 1995
Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndromeM Oldridge, A O Wilkie, S F Slaney, et al.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.
Nature Genetics|November 5, 1997
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domainR J Gibbons, S Bachoo, D J Picketts, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Nature Genetics|May 1, 1996
Exclusive paternal origin of new mutations in Apert syndromeD M Moloney, S F Slaney, M Oldridge, et al.
Journal of Medical Genetics|September 1, 1994
Asymmetry and skin pigmentary anomalies in chromosome mosaicismC G Woods, A Bankier, J Curry, et al.
American Journal of Human Genetics|May 1, 1996
Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndromeS F Slaney, M Oldridge, J A Hurst, et al.
Nature Genetics|February 1, 1995
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypesP Rutland, L J Pulleyn, W Reardon, et al.
Archives of Disease in Childhood|January 1, 1995
DNA testing for fragile X syndrome in schools for learning difficultiesS F Slaney, A O Wilkie, M C Hirst, et al.
Nature Genetics|February 1, 1995
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndromeA O Wilkie, S F Slaney, M Oldridge, et al.
Human Molecular Genetics|June 1, 1995
Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndromeM Oldridge, A O Wilkie, S F Slaney, et al.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.
Nature Genetics|November 5, 1997
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domainR J Gibbons, S Bachoo, D J Picketts, et al.
Pageof 2