J M Opitz|E F Gilbert-Barness - JoVE Visualize

Showing results (151-160 of 177) with videos related to

Pageof 18

Sort By:

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.

American Journal of Medical Genetics|July 16, 1999

Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.

American Journal of Medical Genetics|January 1, 1991

A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, 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. 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.

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.

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.

American Journal of Medical Genetics|May 1, 1983

Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.

Pageof 18

Showing results (151-160 of 177) with videos related to

Sort By:

Pageof 18

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.

American Journal of Medical Genetics|July 16, 1999

Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.

American Journal of Medical Genetics|January 1, 1991

A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, 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. 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.

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.

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.

American Journal of Medical Genetics|May 1, 1983

Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.

Pageof 18