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European Journal of Pediatrics|October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 casesA L Kosseff, J Herrmann, E F Gilbert, et al.
American Journal of Medical Genetics|April 14, 1997
Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian familyG Sorge, L Pavone, A Polizzi, et al.
European Journal of Pediatrics|January 2, 1976
Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.
American Journal of Medical Genetics|November 1, 1994
Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional casesB Angle, S Holgado, B K Burton, et al.
European Journal of Pediatrics|August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
Pediatric Pathology|January 1, 1985
Familial hemophagocytic lymphohistiocytosis: report of four cases in two families and review of the literatureE F Gilbert, G M ZuRhein, S M Wester, et al.
European Journal of Pediatrics|August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest diseaseL O Langer, M Gonzalez-Ramos, H Chen, et al.
American Journal of Medical Genetics|January 1, 1980
Multiple pterygium syndromeH Chen, C H Chang, R P Misra, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
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