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J V Higgins

Showing results (11-20 of 82) with videos related to

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Human Genetics|December 18, 1978
Partial trisomy 2q and familial translocation t(2;18)(q31;p11)L Wisniewski, R Chan, J V Higgins
Clinical Dysmorphology|October 1, 1995
Oculoauriculofrontonasal syndrome: report of another case and review of differential diagnosisH V Toriello, J V Higgins, R Mann
American Journal of Medical Genetics|October 1, 1993
Provisionally unique autosomal recessive chondrodysplasia punctata syndromeH V Toriello, J V Higgins, T Miller
Current Opinion in Plant Biology|April 19, 2002
Plasticity of seed protein composition in response to nitrogen and sulfur availabilityLinda Tabe, Nicholas Hagan, T J V Higgins
Clinical Genetics|September 1, 1978
Partial tetrasomy 9 in a liveborn infantL Wisniewski, G D Politis, J V Higgins
American Journal of Medical Genetics|May 1, 1983
Autosomal-recessive aplasia cutis congenita--report of two affected sibsH V Toriello, J V Higgins, D F Waterman
American Journal of Diseases of Children (1960)|February 1, 1977
A syndrome of microcephaly and cataracts in four siblings. A new genetic syndrome?A B Scott-Emuakpor, J Heffelfinger, J V Higgins
Human Genetics|September 1, 1979
Cytogenetic and clinical studies in five cases of inv dup(15)L Wisniewski, T Hassold, J Heffelfinger, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1977
Ovarian dysgenesis due to 45 X, 0/46 dic (X) mosaicismL J Valenta, J V Higgins, G B Holzman
American Journal of Medical Genetics|February 1, 1987
Menkes syndrome in a girl with X-autosome translocationS Kapur, J V Higgins, K Delp, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
Human Genetics|December 18, 1978
Partial trisomy 2q and familial translocation t(2;18)(q31;p11)L Wisniewski, R Chan, J V Higgins
Clinical Dysmorphology|October 1, 1995
Oculoauriculofrontonasal syndrome: report of another case and review of differential diagnosisH V Toriello, J V Higgins, R Mann
American Journal of Medical Genetics|October 1, 1993
Provisionally unique autosomal recessive chondrodysplasia punctata syndromeH V Toriello, J V Higgins, T Miller
Current Opinion in Plant Biology|April 19, 2002
Plasticity of seed protein composition in response to nitrogen and sulfur availabilityLinda Tabe, Nicholas Hagan, T J V Higgins
Clinical Genetics|September 1, 1978
Partial tetrasomy 9 in a liveborn infantL Wisniewski, G D Politis, J V Higgins
American Journal of Medical Genetics|May 1, 1983
Autosomal-recessive aplasia cutis congenita--report of two affected sibsH V Toriello, J V Higgins, D F Waterman
American Journal of Diseases of Children (1960)|February 1, 1977
A syndrome of microcephaly and cataracts in four siblings. A new genetic syndrome?A B Scott-Emuakpor, J Heffelfinger, J V Higgins
Human Genetics|September 1, 1979
Cytogenetic and clinical studies in five cases of inv dup(15)L Wisniewski, T Hassold, J Heffelfinger, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1977
Ovarian dysgenesis due to 45 X, 0/46 dic (X) mosaicismL J Valenta, J V Higgins, G B Holzman
American Journal of Medical Genetics|February 1, 1987
Menkes syndrome in a girl with X-autosome translocationS Kapur, J V Higgins, K Delp, et al.
Pageof 9