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J M Opitz

Showing results (301-310 of 338) with videos related to

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American Journal of Medical Genetics|September 1, 1985
Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduriaM D Haust, B A Gordon, R Hong, et al.
Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.
Birth Defects Original Article Series|January 1, 1974
Familial cardiac lipidosisJ S Deacon, E F Gilbert, C Viseskul, et al.
American Journal of Medical Genetics. Part A|May 16, 2003
Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patientsM I Kavamura, M Zollino, R Lecce, et al.
American Journal of Medical Genetics|October 1, 1990
GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the olderA Wajntal, C P Koiffmann, B B Mendonça, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1975
Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and reviewR J Hodach, C Viseskul, E F Gilbert, et al.
American Journal of Medical Genetics|February 13, 1995
Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defectG Sorge, S Ardito, M Genuardi, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
American Journal of Medical Genetics|January 1, 1983
A fifty-year-old man with skin pigmentation, arthritis, chronic renal failure and methemoglobinemiaK Abreo, F Abreo, S W Zimmerman, et al.
Zeitschrift Fur Kinderheilkunde|September 11, 1975
Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural studyE F Gilbert, J Varakis, J M Opitz, et al.
Pageof 34

Showing results (301-310 of 338) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics|September 1, 1985
Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduriaM D Haust, B A Gordon, R Hong, et al.
Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.
Birth Defects Original Article Series|January 1, 1974
Familial cardiac lipidosisJ S Deacon, E F Gilbert, C Viseskul, et al.
American Journal of Medical Genetics. Part A|May 16, 2003
Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patientsM I Kavamura, M Zollino, R Lecce, et al.
American Journal of Medical Genetics|October 1, 1990
GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the olderA Wajntal, C P Koiffmann, B B Mendonça, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1975
Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and reviewR J Hodach, C Viseskul, E F Gilbert, et al.
American Journal of Medical Genetics|February 13, 1995
Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defectG Sorge, S Ardito, M Genuardi, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
American Journal of Medical Genetics|January 1, 1983
A fifty-year-old man with skin pigmentation, arthritis, chronic renal failure and methemoglobinemiaK Abreo, F Abreo, S W Zimmerman, et al.
Zeitschrift Fur Kinderheilkunde|September 11, 1975
Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural studyE F Gilbert, J Varakis, J M Opitz, et al.
Pageof 34