Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J M Opitz

Showing results (201-210 of 338) with videos related to

Pageof 34
Sort By:
American Journal of Medical Genetics. Part A|October 30, 2013
Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. 1988G Neri, R Marini, M Cappa, et al.
American Journal of Medical Genetics|August 3, 2001
Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18G Chamyan, D Debich-Spicer, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1985
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from MontanaJ M Opitz, R B Lowry, T M Holmes, et al.
European Journal of Pediatrics|July 1, 1977
Studies of malformation syndromes of man XLVII: disappearance of spermatogonia in the Fanconi anemia syndromeG J Bargman, N T Shahidi, E F Gilbert, et al.
American Journal of Medical Genetics|November 1, 1987
Smith-Lemli-Opitz (RSH) syndrome bibliographyJ M Opitz, V B Penchaszadeh, M C Holt, et al.
American Journal of Medical Genetics|November 1, 1985
NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndromeA Daniel, L Ekblom, S Phillips, et al.
American Journal of Medical Genetics|October 1, 1987
Sudden death in childhood in a case of the G syndromeS L Einfeld, M J Fairley, B F Green, et al.
European Journal of Pediatrics|February 21, 1977
Hemihypotrophy in a girl with a translocation t(13q;7p)F A Marçallo, L C Werneck, R F Pilotto, et al.
Clinical Genetics|May 1, 1975
The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndromeK W Gilchrist, E F Gilbert, N T Shahidi, et al.
American Journal of Medical Genetics|September 1, 1984
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomaliesG Neri, M E Martini-Neri, B E Katz, et al.
Pageof 34

Showing results (201-210 of 338) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics. Part A|October 30, 2013
Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. 1988G Neri, R Marini, M Cappa, et al.
American Journal of Medical Genetics|August 3, 2001
Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18G Chamyan, D Debich-Spicer, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1985
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from MontanaJ M Opitz, R B Lowry, T M Holmes, et al.
European Journal of Pediatrics|July 1, 1977
Studies of malformation syndromes of man XLVII: disappearance of spermatogonia in the Fanconi anemia syndromeG J Bargman, N T Shahidi, E F Gilbert, et al.
American Journal of Medical Genetics|November 1, 1987
Smith-Lemli-Opitz (RSH) syndrome bibliographyJ M Opitz, V B Penchaszadeh, M C Holt, et al.
American Journal of Medical Genetics|November 1, 1985
NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndromeA Daniel, L Ekblom, S Phillips, et al.
American Journal of Medical Genetics|October 1, 1987
Sudden death in childhood in a case of the G syndromeS L Einfeld, M J Fairley, B F Green, et al.
European Journal of Pediatrics|February 21, 1977
Hemihypotrophy in a girl with a translocation t(13q;7p)F A Marçallo, L C Werneck, R F Pilotto, et al.
Clinical Genetics|May 1, 1975
The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndromeK W Gilchrist, E F Gilbert, N T Shahidi, et al.
American Journal of Medical Genetics|September 1, 1984
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomaliesG Neri, M E Martini-Neri, B E Katz, et al.
Pageof 34