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C P Bennett

Showing results (1-10 of 17) with videos related to

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The Hospital and Health Services Review|March 13, 1978
Operational research and transport arrangements in an AHAC P Bennett, I B Duncan
American Journal of Medical Genetics|October 1, 1990
Pseudotrisomy 13 syndromeM J Seller, C P Bennett
Journal of Medical Genetics|October 1, 1992
Trisomy 15 mosaicism in an IVF fetusC P Bennett, T Davis, M J Seller
Clinical Dysmorphology|October 1, 1994
Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS)A J Barnicoat, M J Seller, C P Bennett
American Journal of Medical Genetics|May 8, 1999
Duplication involving band 4q32 with minimal clinical effectE L Maltby, I C Barnes, C P Bennett
Journal of Medical Genetics|April 1, 1991
Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalitiesC P Bennett, D R Betts, M J Seller
American Journal of Medical Genetics|December 1, 1992
Chondrodysplasia punctata: another possible X-linked recessive caseC P Bennett, A C Berry, D J Maxwell, et al.
Clinical Genetics|August 1, 1989
Holoprosencephaly, polydactyly and normal chromosomes: pseudo-trisomy 13?B G Hewitt, M J Seller, C P Bennett, et al.
Journal of Medical Genetics|September 1, 1995
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255C P Bennett, A J Barnicoat, F Cotter, et al.
Journal of Medical Genetics|May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosisC P Bennett, J Burn, G E Moore, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
The Hospital and Health Services Review|March 13, 1978
Operational research and transport arrangements in an AHAC P Bennett, I B Duncan
American Journal of Medical Genetics|October 1, 1990
Pseudotrisomy 13 syndromeM J Seller, C P Bennett
Journal of Medical Genetics|October 1, 1992
Trisomy 15 mosaicism in an IVF fetusC P Bennett, T Davis, M J Seller
Clinical Dysmorphology|October 1, 1994
Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS)A J Barnicoat, M J Seller, C P Bennett
American Journal of Medical Genetics|May 8, 1999
Duplication involving band 4q32 with minimal clinical effectE L Maltby, I C Barnes, C P Bennett
Journal of Medical Genetics|April 1, 1991
Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalitiesC P Bennett, D R Betts, M J Seller
American Journal of Medical Genetics|December 1, 1992
Chondrodysplasia punctata: another possible X-linked recessive caseC P Bennett, A C Berry, D J Maxwell, et al.
Clinical Genetics|August 1, 1989
Holoprosencephaly, polydactyly and normal chromosomes: pseudo-trisomy 13?B G Hewitt, M J Seller, C P Bennett, et al.
Journal of Medical Genetics|September 1, 1995
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255C P Bennett, A J Barnicoat, F Cotter, et al.
Journal of Medical Genetics|May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosisC P Bennett, J Burn, G E Moore, et al.
Pageof 2