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J M Opitz

Showing results (311-320 of 338) with videos related to

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Birth Defects Original Article Series|January 1, 1977
The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemiaC H Gonzalez, M V Durkin-Stamm, N F Geimer, et al.
American Journal of Medical Genetics|May 1, 1983
Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.
The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatmentF Lalatta, D Clerici Bagozzi, M G Salmoiraghi, et al.
American Journal of Medical Genetics|May 1, 1983
The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971C S Houston, J M Opitz, J W Spranger, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1974
Generalized lymphangiectosis associated with chylothorax; a possible dysplasia of the lymphatic systemC K Chang, C Viseskul, J M Opitz, et al.
American Journal of Medical Genetics|March 2, 1999
Levels of unconjugated estriol and other maternal serum markers in pregnancies with Smith-Lemli-Opitz (RSH) syndrome fetusesL A Bradley, G E Palomaki, G J Knight, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndromeM I Kavamura, M G Pomponi, M Zollino, et al.
American Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.
Birth Defects Original Article Series|January 1, 1977
The pallister mosaic syndromeP D Pallister, L F Meisner, B R Elejalde, et al.
Pageof 34

Showing results (311-320 of 338) with videos related to

Sort By:
Pageof 34
Birth Defects Original Article Series|January 1, 1977
The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemiaC H Gonzalez, M V Durkin-Stamm, N F Geimer, et al.
American Journal of Medical Genetics|May 1, 1983
Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.
The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatmentF Lalatta, D Clerici Bagozzi, M G Salmoiraghi, et al.
American Journal of Medical Genetics|May 1, 1983
The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971C S Houston, J M Opitz, J W Spranger, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1974
Generalized lymphangiectosis associated with chylothorax; a possible dysplasia of the lymphatic systemC K Chang, C Viseskul, J M Opitz, et al.
American Journal of Medical Genetics|March 2, 1999
Levels of unconjugated estriol and other maternal serum markers in pregnancies with Smith-Lemli-Opitz (RSH) syndrome fetusesL A Bradley, G E Palomaki, G J Knight, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndromeM I Kavamura, M G Pomponi, M Zollino, et al.
American Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.
Birth Defects Original Article Series|January 1, 1977
The pallister mosaic syndromeP D Pallister, L F Meisner, B R Elejalde, et al.
Pageof 34