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C N Fear

Showing results (1-10 of 8) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1978
A 1q translocation family segregating for peptidase CP J Cook, C N Fear, S Povey
Journal of Medical Genetics|October 1, 1986
Three children with partial trisomy 1q and partial monosomy 3pG T McCarthy, C N Fear, A C Berry
Clinical Genetics|April 1, 1989
A 45,X/69,XXY fetusD R Betts, C N Fear, T Barby, et al.
Lancet (London, England)|April 4, 1981
Fragile X in a normal male: a cautionary taleM G Daker, P Chidiac, C N Fear, et al.
Developmental Medicine and Child Neurology|June 1, 1985
Chromosome 15 in Prader-Willi syndromeC N Fear, D E Mutton, A C Berry, et al.
Journal of Medical Genetics|February 1, 1991
Two cases of interstitial deletion 1pM M Lai, M F Robards, A C Berry, et al.
American Journal of Medical Genetics|March 29, 1996
Two sibs with anophthalmia and pulmonary hypoplasia (the Matthew-Wood syndrome)M J Seller, T B Davis, C N Fear, et al.
Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Cytogenetics and Cell Genetics|January 1, 1978
A 1q translocation family segregating for peptidase CP J Cook, C N Fear, S Povey
Journal of Medical Genetics|October 1, 1986
Three children with partial trisomy 1q and partial monosomy 3pG T McCarthy, C N Fear, A C Berry
Clinical Genetics|April 1, 1989
A 45,X/69,XXY fetusD R Betts, C N Fear, T Barby, et al.
Lancet (London, England)|April 4, 1981
Fragile X in a normal male: a cautionary taleM G Daker, P Chidiac, C N Fear, et al.
Developmental Medicine and Child Neurology|June 1, 1985
Chromosome 15 in Prader-Willi syndromeC N Fear, D E Mutton, A C Berry, et al.
Journal of Medical Genetics|February 1, 1991
Two cases of interstitial deletion 1pM M Lai, M F Robards, A C Berry, et al.
American Journal of Medical Genetics|March 29, 1996
Two sibs with anophthalmia and pulmonary hypoplasia (the Matthew-Wood syndrome)M J Seller, T B Davis, C N Fear, et al.
Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.
Pageof 1