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J M Opitz

Showing results (231-240 of 338) with videos related to

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American Journal of Medical Genetics|May 1, 1988
FG syndrome update 1988: note of 5 new patients and bibliographyJ M Opitz, A Richieri-da Costa, J M Aase, et al.
Lancet (London, England)|February 2, 1974
Letter: Immunodeficiency in the cerebro-hepato-renal syndrome of ZellwegerK W Gilkrist, J M Opitz, E F Gilbert, et al.
Pediatrics|April 1, 1973
X-linked aqueductal stenosis: clinical and neuropathological findings in two familiesL B Holmes, A Nash, G M ZuRhein, et al.
Clinical Dysmorphology|January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in picturesA Battaglia, J C Carey, D H Viskochil, et al.
American Journal of Medical Genetics|January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosisR Rizzo, V Pavone, G Corsello, et al.
American Journal of Medical Genetics|January 1, 1978
An unusual dysplasia-malformation-cancer syndrome in two patientsM V Durkin-Stamm, E F Gilbert, D J Ganick, et al.
Birth Defects Original Article Series|January 1, 1974
Arthrodentoosteodysplasia: a genetic "acroosteolysis" syndromeF T Zugibe, J Herrmann, J M Opitz, et al.
Lancet (London, England)|February 21, 1976
Letter: Trisomy-20 syndrome in manP D Pallister, J Herrmann, L F Meisner, et al.
American Journal of Medical Genetics|March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studiesJ M Opitz, J W Spranger, H R Stöss, et al.
American Journal of Medical Genetics|June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collectionA Utkus, R Kazakevicius, R Ptasekas, et al.
Pageof 34

Showing results (231-240 of 338) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics|May 1, 1988
FG syndrome update 1988: note of 5 new patients and bibliographyJ M Opitz, A Richieri-da Costa, J M Aase, et al.
Lancet (London, England)|February 2, 1974
Letter: Immunodeficiency in the cerebro-hepato-renal syndrome of ZellwegerK W Gilkrist, J M Opitz, E F Gilbert, et al.
Pediatrics|April 1, 1973
X-linked aqueductal stenosis: clinical and neuropathological findings in two familiesL B Holmes, A Nash, G M ZuRhein, et al.
Clinical Dysmorphology|January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in picturesA Battaglia, J C Carey, D H Viskochil, et al.
American Journal of Medical Genetics|January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosisR Rizzo, V Pavone, G Corsello, et al.
American Journal of Medical Genetics|January 1, 1978
An unusual dysplasia-malformation-cancer syndrome in two patientsM V Durkin-Stamm, E F Gilbert, D J Ganick, et al.
Birth Defects Original Article Series|January 1, 1974
Arthrodentoosteodysplasia: a genetic "acroosteolysis" syndromeF T Zugibe, J Herrmann, J M Opitz, et al.
Lancet (London, England)|February 21, 1976
Letter: Trisomy-20 syndrome in manP D Pallister, J Herrmann, L F Meisner, et al.
American Journal of Medical Genetics|March 1, 1987
Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studiesJ M Opitz, J W Spranger, H R Stöss, et al.
American Journal of Medical Genetics|June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collectionA Utkus, R Kazakevicius, R Ptasekas, et al.
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