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American Journal of Medical Genetics|September 15, 1992
Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndromeF Martino, P D'Eufemia, M S Pergola, et al.American Journal of Medical Genetics|November 1, 1991
Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalusR F Stratton, D L BluestoneAmerican Journal of Medical Genetics|November 1, 1991
Goldberg-Shprintzen syndrome: Hirschsprung disease, hypotonia, and ptosis in sibsA Yomo, T Taira, I KondoAmerican Journal of Medical Genetics|November 1, 1991
Cognitive and motor skills in achondroplastic infants: neurologic and respiratory correlatesJ T Hecht, N M Thompson, T Weir, et al.American Journal of Medical Genetics|November 1, 1991
Prevalence of type I spinal muscular atrophy in North DakotaL Burd, S K Short, J T Martsolf, et al.American Journal of Medical Genetics|November 1, 1991
Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndromeM Clementi, R Tenconi, L Turolla, et al.American Journal of Medical Genetics|April 1, 1991
Prenatal diagnosis of hereditary amyloidosis in a Portuguese familyM Morris, W Nichols, M BensonAmerican Journal of Medical Genetics|April 1, 1991
Maternal muscle biopsy in X-linked recessive centronuclear (myotubular) myopathyG N Breningstall, W D Grover, H G MarksAmerican Journal of Medical Genetics|April 1, 1991
45,X/47,XYY mosaicism: clinical discrepancy between prenatally and postnatally diagnosed casesM J Pettenati, M Wheeler, D J Bartlett, et al.American Journal of Medical Genetics|April 11, 1991
Deletion of 20p 11.23----pter with normal growth hormone-releasing hormone genesM Shohat, V Herman, S Melmed, et al.Pageof 854