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S M Huson

Showing results (31-40 of 85) with videos related to

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American Journal of Human Genetics|August 1, 1993
An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genesD F Easton, M A Ponder, S M Huson, et al.
Journal of Medical Genetics|June 1, 1990
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndromeS M Huson, C S Rodgers, C M Hall, et al.
Journal of Medical Genetics|October 22, 2003
Evaluation of genotype-phenotype correlations in neurofibromatosis type 1B Castle, M E Baser, S M Huson, et al.
Lancet (London, England)|May 18, 1996
Limb defects and chorionic villus samplingH Firth, P A Boyd, P Chamberlain, et al.
The Journal of Urology|March 21, 2001
von Hippel-Lindau disease: renal tumors less than 3 cm. can metastasizeK J Turner, S M Huson, N Moore, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1994
Incorrect diagnosis of myotonic dystrophy and its potential consequences revealed by subsequent direct genetic analysisP R Barnes, D Hilton-Jones, G Norbury, et al.
Clinical Dysmorphology|January 1, 1993
Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic faciesS M Huson, S Crowley, C M Hall, et al.
Journal of Medical Genetics|December 14, 1999
Unusual clustering of brain tumours in a family with NF1 and variable expression of cutaneous featuresF Faravelli, M Upadhyaya, M Osborn, et al.
Genomics|December 1, 1987
Chromosome 17 markers and von Recklinghausen neurofibromatosis: a genetic linkage study in a British populationM Upadhyaya, M Sarfarazi, S M Huson, et al.
American Journal of Human Genetics|January 1, 1989
Close flanking markers for neurofibromatosis type I (NF1)M Upadhyaya, M Sarfarazi, S M Huson, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|August 1, 1993
An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genesD F Easton, M A Ponder, S M Huson, et al.
Journal of Medical Genetics|June 1, 1990
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndromeS M Huson, C S Rodgers, C M Hall, et al.
Journal of Medical Genetics|October 22, 2003
Evaluation of genotype-phenotype correlations in neurofibromatosis type 1B Castle, M E Baser, S M Huson, et al.
Lancet (London, England)|May 18, 1996
Limb defects and chorionic villus samplingH Firth, P A Boyd, P Chamberlain, et al.
The Journal of Urology|March 21, 2001
von Hippel-Lindau disease: renal tumors less than 3 cm. can metastasizeK J Turner, S M Huson, N Moore, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1994
Incorrect diagnosis of myotonic dystrophy and its potential consequences revealed by subsequent direct genetic analysisP R Barnes, D Hilton-Jones, G Norbury, et al.
Clinical Dysmorphology|January 1, 1993
Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic faciesS M Huson, S Crowley, C M Hall, et al.
Journal of Medical Genetics|December 14, 1999
Unusual clustering of brain tumours in a family with NF1 and variable expression of cutaneous featuresF Faravelli, M Upadhyaya, M Osborn, et al.
Genomics|December 1, 1987
Chromosome 17 markers and von Recklinghausen neurofibromatosis: a genetic linkage study in a British populationM Upadhyaya, M Sarfarazi, S M Huson, et al.
American Journal of Human Genetics|January 1, 1989
Close flanking markers for neurofibromatosis type I (NF1)M Upadhyaya, M Sarfarazi, S M Huson, et al.
Pageof 9