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E F Gilbert

Showing results (201-210 of 218) with videos related to

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American Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.
Clinical Neuropathology|January 1, 1990
Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA)S M Chou, E F Gilbert, R W Chun, et al.
Birth Defects Original Article Series|January 1, 1974
Familial cardiac lipidosisJ S Deacon, E F Gilbert, C Viseskul, et al.
The Journal of Pediatrics|May 1, 1973
Immunodeficiency associated with exomphalos-macroglossia-gigantism syndromeR J Greene, E F Gilbert, S W Huang, et al.
Journal of Applied Toxicology : JAT|February 1, 1988
The effects of caffeine on the ultrastructure and mitochondrial function of the embryonic chick heartH J Bruyere, J J Noonan, S Dong, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1975
Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and reviewR J Hodach, C Viseskul, E F Gilbert, et al.
The New England Journal of Medicine|August 13, 1981
Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathyM E Tripp, M L Katcher, H A Peters, et al.
American Journal of Medical Genetics|January 1, 1983
A fifty-year-old man with skin pigmentation, arthritis, chronic renal failure and methemoglobinemiaK Abreo, F Abreo, S W Zimmerman, et al.
Zeitschrift Fur Kinderheilkunde|September 11, 1975
Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural studyE F Gilbert, J Varakis, J M Opitz, et al.
American Journal of Medical Genetics|May 1, 1983
Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.
Pageof 22

Showing results (201-210 of 218) with videos related to

Sort By:
Pageof 22
American Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.
Clinical Neuropathology|January 1, 1990
Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA)S M Chou, E F Gilbert, R W Chun, et al.
Birth Defects Original Article Series|January 1, 1974
Familial cardiac lipidosisJ S Deacon, E F Gilbert, C Viseskul, et al.
The Journal of Pediatrics|May 1, 1973
Immunodeficiency associated with exomphalos-macroglossia-gigantism syndromeR J Greene, E F Gilbert, S W Huang, et al.
Journal of Applied Toxicology : JAT|February 1, 1988
The effects of caffeine on the ultrastructure and mitochondrial function of the embryonic chick heartH J Bruyere, J J Noonan, S Dong, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1975
Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and reviewR J Hodach, C Viseskul, E F Gilbert, et al.
The New England Journal of Medicine|August 13, 1981
Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathyM E Tripp, M L Katcher, H A Peters, et al.
American Journal of Medical Genetics|January 1, 1983
A fifty-year-old man with skin pigmentation, arthritis, chronic renal failure and methemoglobinemiaK Abreo, F Abreo, S W Zimmerman, et al.
Zeitschrift Fur Kinderheilkunde|September 11, 1975
Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural studyE F Gilbert, J Varakis, J M Opitz, et al.
American Journal of Medical Genetics|May 1, 1983
Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.
Pageof 22