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J L Tolmie

Showing results (31-40 of 72) with videos related to

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American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.
Prenatal Diagnosis|October 1, 1987
Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicismJ L Tolmie, M E Ferguson-Smith, D Gilmore, et al.
Human Genetics|January 1, 1990
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determinationM A Ferguson-Smith, A Cooke, N A Affara, et al.
Clinical Dysmorphology|January 1, 1993
Severe prenatal infantile cortical hyperostosis (Caffey's disease)P D Turnpenny, R Davidson, E J Stockdale, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Hurler-Scheie phenotype associated with consanguinityD L Davies, G N Dutton, J Farquharson, et al.
American Journal of Medical Genetics|May 1, 1987
The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sibJ L Tolmie, G Mortimer, D Doyle, et al.
Journal of Medical Genetics|October 23, 1998
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisationS R Ghaffari, E Boyd, J M Connor, et al.
Human Genetics|August 1, 1989
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometryA Cooke, J L Tolmie, J M Colgan, et al.
Clinical Dysmorphology|April 20, 2001
A new case of Myhre syndromeM L Whiteford, W B Doig, P A Raine, et al.
Journal of Medical Genetics|March 1, 1996
Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular studyE Reid, N Morrison, L Barron, et al.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.
Prenatal Diagnosis|October 1, 1987
Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicismJ L Tolmie, M E Ferguson-Smith, D Gilmore, et al.
Human Genetics|January 1, 1990
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determinationM A Ferguson-Smith, A Cooke, N A Affara, et al.
Clinical Dysmorphology|January 1, 1993
Severe prenatal infantile cortical hyperostosis (Caffey's disease)P D Turnpenny, R Davidson, E J Stockdale, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Hurler-Scheie phenotype associated with consanguinityD L Davies, G N Dutton, J Farquharson, et al.
American Journal of Medical Genetics|May 1, 1987
The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sibJ L Tolmie, G Mortimer, D Doyle, et al.
Journal of Medical Genetics|October 23, 1998
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisationS R Ghaffari, E Boyd, J M Connor, et al.
Human Genetics|August 1, 1989
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometryA Cooke, J L Tolmie, J M Colgan, et al.
Clinical Dysmorphology|April 20, 2001
A new case of Myhre syndromeM L Whiteford, W B Doig, P A Raine, et al.
Journal of Medical Genetics|March 1, 1996
Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular studyE Reid, N Morrison, L Barron, et al.
Pageof 8