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D M Parry

Showing results (71-80 of 79) with videos related to

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American Journal of Diseases of Children (1960)|July 1, 1989
Neurofibromatosis type 1 (Recklinghausen's disease). Neurologic and cognitive assessment with sibling controlsR Eldridge, M B Denckla, E Bien, et al.
Cell|March 12, 1993
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressorJ A Trofatter, M M MacCollin, J L Rutter, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1987
Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcomaC Turc-Carel, P Dal Cin, J Limon, et al.
American Journal of Human Genetics|January 1, 1989
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)B R Seizinger, G E Farmer, J L Haines, et al.
Genetic Epidemiology|October 18, 2002
Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2)Y Zhao, R A Kumar, M E Baser, et al.
Genomics|December 1, 1987
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17B R Seizinger, G A Rouleau, A H Lane, et al.
Cell|June 5, 1987
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor geneB R Seizinger, G A Rouleau, L J Ozelius, et al.
Journal of Medical Genetics|July 5, 2005
The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2M E Baser, L Kuramoto, R Woods, et al.
Genetics|May 1, 1972
Segmental aneuploidy and the genetic gross structure of the Drosophila genomeD L Lindsley, L Sandler, B S Baker, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
American Journal of Diseases of Children (1960)|July 1, 1989
Neurofibromatosis type 1 (Recklinghausen's disease). Neurologic and cognitive assessment with sibling controlsR Eldridge, M B Denckla, E Bien, et al.
Cell|March 12, 1993
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressorJ A Trofatter, M M MacCollin, J L Rutter, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1987
Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcomaC Turc-Carel, P Dal Cin, J Limon, et al.
American Journal of Human Genetics|January 1, 1989
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)B R Seizinger, G E Farmer, J L Haines, et al.
Genetic Epidemiology|October 18, 2002
Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2)Y Zhao, R A Kumar, M E Baser, et al.
Genomics|December 1, 1987
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17B R Seizinger, G A Rouleau, A H Lane, et al.
Cell|June 5, 1987
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor geneB R Seizinger, G A Rouleau, L J Ozelius, et al.
Journal of Medical Genetics|July 5, 2005
The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2M E Baser, L Kuramoto, R Woods, et al.
Genetics|May 1, 1972
Segmental aneuploidy and the genetic gross structure of the Drosophila genomeD L Lindsley, L Sandler, B S Baker, et al.
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