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R Weksberg

Showing results (31-40 of 84) with videos related to

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Journal of Genetic Counseling|August 12, 2015
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic CounselingR Z Hayeems, R Babul-Hirji, N Hoang, et al.
Neurosurgery|July 1, 1995
Absence of the greater sphenoid wing in neurofibromatosis type I: congenital or acquired: case reportR Macfarlane, A V Levin, R Weksberg, et al.
Nature Genetics|October 1, 1993
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndromeR Weksberg, D R Shen, Y L Fei, et al.
American Journal of Medical Genetics|March 25, 1998
MRI findings in macrocephaly-cutis marmorata telangiectatica congenitaM Carcao, S I Blaser, R M Grant, et al.
Journal of Medical Genetics|May 1, 1996
Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasiaL E Bernard, D Chitayat, R Weksberg, et al.
Genomics|December 1, 1990
Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS regionR Weksberg, M Glaves, I Teshima, et al.
American Journal of Medical Genetics|January 23, 2002
Patterns of dysmorphic features in schizophreniaL E Scutt, E W Chow, R Weksberg, et al.
Human Genetics|January 1, 1983
A dominantly inherited cytogenetic anomaly: a possible cell division mutantN L Rudd, I E Teshima, R H Martin, et al.
American Journal of Medical Genetics|July 23, 1998
Schimke immunoosseous dysplasia complicated by moyamoya phenomenonC F Boerkoel, M J Nowaczyk, S I Blaser, et al.
The Journal of Pediatrics|May 1, 1993
Wilms tumor in a patient with Prader-Willi syndromeM J Coppes, H Sohl, I E Teshima, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Journal of Genetic Counseling|August 12, 2015
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic CounselingR Z Hayeems, R Babul-Hirji, N Hoang, et al.
Neurosurgery|July 1, 1995
Absence of the greater sphenoid wing in neurofibromatosis type I: congenital or acquired: case reportR Macfarlane, A V Levin, R Weksberg, et al.
Nature Genetics|October 1, 1993
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndromeR Weksberg, D R Shen, Y L Fei, et al.
American Journal of Medical Genetics|March 25, 1998
MRI findings in macrocephaly-cutis marmorata telangiectatica congenitaM Carcao, S I Blaser, R M Grant, et al.
Journal of Medical Genetics|May 1, 1996
Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasiaL E Bernard, D Chitayat, R Weksberg, et al.
Genomics|December 1, 1990
Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS regionR Weksberg, M Glaves, I Teshima, et al.
American Journal of Medical Genetics|January 23, 2002
Patterns of dysmorphic features in schizophreniaL E Scutt, E W Chow, R Weksberg, et al.
Human Genetics|January 1, 1983
A dominantly inherited cytogenetic anomaly: a possible cell division mutantN L Rudd, I E Teshima, R H Martin, et al.
American Journal of Medical Genetics|July 23, 1998
Schimke immunoosseous dysplasia complicated by moyamoya phenomenonC F Boerkoel, M J Nowaczyk, S I Blaser, et al.
The Journal of Pediatrics|May 1, 1993
Wilms tumor in a patient with Prader-Willi syndromeM J Coppes, H Sohl, I E Teshima, et al.
Pageof 9