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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.Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.American Journal of Medical Genetics|December 8, 1998
Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalangesW R Osebold, A K Poznanski, J M Opitz, et al.European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndromeJ Herrmann, P D Pallister, E F Gilbert, et al.Journal of Medical Genetics|September 1, 1975
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signsN Freire-Maia, V A Fortes, L C Pereira, et al.The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa functionS Pang, L S Levine, E Stoner, et al.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.Pageof 17