J M Opitz|M C Holt - JoVE Visualize

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American Journal of Medical Genetics|November 1, 1986

New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndromeJ F Reynolds, G Neri, J P Herrmann, et al.

American Journal of Medical Genetics. Supplement|January 1, 1987

The Montana Fetal Genetic Pathology Program and a review of prenatal death in humansJ M Opitz, J M FitzGerald, J F Reynolds, 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.

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.

Pageof 17

Showing results (141-150 of 170) with videos related to

Sort By:

Pageof 17

American Journal of Medical Genetics|November 1, 1986

New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndromeJ F Reynolds, G Neri, J P Herrmann, et al.

American Journal of Medical Genetics. Supplement|January 1, 1987

The Montana Fetal Genetic Pathology Program and a review of prenatal death in humansJ M Opitz, J M FitzGerald, J F Reynolds, 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.

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.

Pageof 17