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American Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.Journal of Medical Genetics|July 11, 2006
The cardiofaciocutaneous syndromeA Roberts, J Allanson, S K Jadico, et al.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.Pageof 19