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M Opitz

Showing results (301-310 of 520) with videos related to

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European Journal of Pediatrics|March 18, 1977
A biologic and genetic study of 40 cases of severe pure mental retardationJ M Becker, E G Kaveggia, E Pendleton, et al.
European Journal of Pediatrics|February 21, 1977
Fatal CNS dysgenesis with severe microencephaly, mental retardation, seizures and paucity of myelin, autosomal recessive trait?G Neuhäuser, G M ZuRhein, E G Kaveggia, et al.
Zeitschrift Fur Kinderheilkunde|April 4, 1973
Arthro-dento-osteo dysplasia (Hajdu-Cheney syndrome). Review of a genetic "acro-osteolysis" syndromeJ Herrmann, F T Zugibe, E F Gilbert, et al.
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.
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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 12, 2003
Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxiaMaria Cristina Digilio, Bruno Marino, Aldo Giannotti, et al.
Fetal and Pediatric Pathology|February 15, 2012
Premature closure of the foramen ovale secondary to congenital aortic valvular stenosis in a stillbornLarissa V Furtado, Angelica R Putnam, Lance K Erickson, 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.
Pageof 52

Showing results (301-310 of 520) with videos related to

Sort By:
Pageof 52
European Journal of Pediatrics|March 18, 1977
A biologic and genetic study of 40 cases of severe pure mental retardationJ M Becker, E G Kaveggia, E Pendleton, et al.
European Journal of Pediatrics|February 21, 1977
Fatal CNS dysgenesis with severe microencephaly, mental retardation, seizures and paucity of myelin, autosomal recessive trait?G Neuhäuser, G M ZuRhein, E G Kaveggia, et al.
Zeitschrift Fur Kinderheilkunde|April 4, 1973
Arthro-dento-osteo dysplasia (Hajdu-Cheney syndrome). Review of a genetic "acro-osteolysis" syndromeJ Herrmann, F T Zugibe, E F Gilbert, et al.
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.
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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 12, 2003
Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxiaMaria Cristina Digilio, Bruno Marino, Aldo Giannotti, et al.
Fetal and Pediatric Pathology|February 15, 2012
Premature closure of the foramen ovale secondary to congenital aortic valvular stenosis in a stillbornLarissa V Furtado, Angelica R Putnam, Lance K Erickson, 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.
Pageof 52