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D D Weaver

Showing results (31-40 of 99) with videos related to

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American Journal of Medical Genetics|February 1, 1989
Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicismR A Helmuth, D D Weaver, E R Wills
American Journal of Human Genetics|July 1, 1970
Discrimination of phenotypes in human serum cholinesterase deficiencyE M Scott, D D Weaver, R C Wright
Archives of Neurology|January 1, 1984
Familial startle disease (hyperexplexia). Electrophysiologic studiesO N Markand, B P Garg, D D Weaver
Journal of Neurosurgery|May 1, 1982
Differential intracranial pressure in patients with unilateral mass lesionsD D Weaver, H R Winn, J A Jane
Human Genetics|January 1, 1982
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle functionE A Keitges, C G Palmer, D D Weaver
Clinical Genetics|November 1, 1982
Prader-Willi syndrome: are there population differences?M G Butler, D D Weaver, F J Meaney
American Journal of Diseases of Children (1960)|December 1, 1977
The fetal trimethadione syndrome: report of an additional family and further delineation of this syndromeG L Feldman, D D Weaver, E W Lovrien
American Journal of Medical Genetics|March 1, 1984
Acrofacial dysostosis with severe facial clefting and limb reductionE L Kawira, D D Weaver, H A Bender
The Journal of Clinical Dysmorphology|January 1, 1983
Syndrome identification case report 95: congenital fusion of the gums and jawsS D Kittur, D D Weaver, M D Maves
Pediatrics|February 1, 1981
The axial mesodermal dysplasia spectrumL J Russell, D D Weaver, M J Bull
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics|February 1, 1989
Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicismR A Helmuth, D D Weaver, E R Wills
American Journal of Human Genetics|July 1, 1970
Discrimination of phenotypes in human serum cholinesterase deficiencyE M Scott, D D Weaver, R C Wright
Archives of Neurology|January 1, 1984
Familial startle disease (hyperexplexia). Electrophysiologic studiesO N Markand, B P Garg, D D Weaver
Journal of Neurosurgery|May 1, 1982
Differential intracranial pressure in patients with unilateral mass lesionsD D Weaver, H R Winn, J A Jane
Human Genetics|January 1, 1982
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle functionE A Keitges, C G Palmer, D D Weaver
Clinical Genetics|November 1, 1982
Prader-Willi syndrome: are there population differences?M G Butler, D D Weaver, F J Meaney
American Journal of Diseases of Children (1960)|December 1, 1977
The fetal trimethadione syndrome: report of an additional family and further delineation of this syndromeG L Feldman, D D Weaver, E W Lovrien
American Journal of Medical Genetics|March 1, 1984
Acrofacial dysostosis with severe facial clefting and limb reductionE L Kawira, D D Weaver, H A Bender
The Journal of Clinical Dysmorphology|January 1, 1983
Syndrome identification case report 95: congenital fusion of the gums and jawsS D Kittur, D D Weaver, M D Maves
Pediatrics|February 1, 1981
The axial mesodermal dysplasia spectrumL J Russell, D D Weaver, M J Bull
Pageof 10