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J M Opitz

Showing results (131-140 of 338) with videos related to

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Birth Defects Original Article Series|October 1, 1970
Anatomic studies in the 18-trisomy syndromeB A Barash, L Freedman, J M Opitz
Pediatric Pathology|January 1, 1985
Omenn disease: termination in lymphomaR Hong, E F Gilbert, J M Opitz
Lancet (London, England)|April 15, 1972
The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic signA L Kosseff, J Herrmann, J M Opitz
Lancet (London, England)|January 8, 1972
Congenital effects of bromism?J M Opitz, F R Grosse, B Haneberg
European Journal of Pediatrics|November 3, 1976
Studies of malformation syndromes of man XXXXIIB: mother and son affected with the ulnar-mammary syndrome type PallisterC H Gonzalez, J Herrmann, J M Opitz
Humangenetik|January 1, 1974
Alpha-aminoadipic aciduria, a non-deleterious inborn metabolic defectM H Fischer, T Gerritsen, J M Opitz
Zeitschrift Fur Kinderheilkunde|January 1, 1975
X-linked hydrocephalus. Further observationsC Viseskul, E F Gilbert, J M Opitz
Humangenetik|January 1, 1971
Heterogeneity of Chondrodysplasia punctataJ W Spranger, J M Opitz, U Bidder
American Journal of Medical Genetics|January 1, 1984
Discovery of a connective tissue dysplasia in the Martin-Bell syndromeJ M Opitz, J M Westphal, A Daniel
Zeitschrift Fur Kinderheilkunde|January 1, 1973
Familial hydronephrosisF R Grosse, L Kaveggia, J M Opitz
Pageof 34

Showing results (131-140 of 338) with videos related to

Sort By:
Pageof 34
Birth Defects Original Article Series|October 1, 1970
Anatomic studies in the 18-trisomy syndromeB A Barash, L Freedman, J M Opitz
Pediatric Pathology|January 1, 1985
Omenn disease: termination in lymphomaR Hong, E F Gilbert, J M Opitz
Lancet (London, England)|April 15, 1972
The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic signA L Kosseff, J Herrmann, J M Opitz
Lancet (London, England)|January 8, 1972
Congenital effects of bromism?J M Opitz, F R Grosse, B Haneberg
European Journal of Pediatrics|November 3, 1976
Studies of malformation syndromes of man XXXXIIB: mother and son affected with the ulnar-mammary syndrome type PallisterC H Gonzalez, J Herrmann, J M Opitz
Humangenetik|January 1, 1974
Alpha-aminoadipic aciduria, a non-deleterious inborn metabolic defectM H Fischer, T Gerritsen, J M Opitz
Zeitschrift Fur Kinderheilkunde|January 1, 1975
X-linked hydrocephalus. Further observationsC Viseskul, E F Gilbert, J M Opitz
Humangenetik|January 1, 1971
Heterogeneity of Chondrodysplasia punctataJ W Spranger, J M Opitz, U Bidder
American Journal of Medical Genetics|January 1, 1984
Discovery of a connective tissue dysplasia in the Martin-Bell syndromeJ M Opitz, J M Westphal, A Daniel
Zeitschrift Fur Kinderheilkunde|January 1, 1973
Familial hydronephrosisF R Grosse, L Kaveggia, J M Opitz
Pageof 34