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American Journal of Medical Genetics|March 15, 1991
Duplication 3q(q21----qter) without limb anomaliesS R Ismail, B G Kousseff, S M Kotb, et al.American Journal of Medical Genetics|March 15, 1991
Interstitial 15q deletion without a classic Prader-Willi phenotypeF Galán, M S Aguilar, J González, et al.American Journal of Medical Genetics|March 15, 1991
The cardio-facio-cutaneous (CFC) syndrome and Noonan syndrome: are they the same?A E Fryer, P J Holt, H E HughesAmerican Journal of Medical Genetics|March 15, 1991
A distinct type of hidrotic ectodermal dysplasiaF Halal, N Setton, N S WangAmerican Journal of Medical Genetics|March 15, 1991
Generalized enchondromatosis in a boy with only platyspondyly in the fatherF Halal, E M AzouzAmerican Journal of Medical Genetics|March 15, 1991
Epidemiological aspects of Mendelian syndromes in a Spanish population sample: II. Autosomal recessive malformation syndromesM L Martínez-Frías, E Bermejo, A Cereijo, et al.American Journal of Medical Genetics|May 1, 1991
X-linked syndrome: mental retardation, hip luxation, and G6PD variant [Gd(+) Butantan]R C dos Santos, O C Barretto, K Nonoyama, et al.American Journal of Medical Genetics|May 1, 1991
Photogrammetric evaluation in clinical genetics: theoretical considerations and experimental resultsJ H DiLiberti, D P OlsonAmerican Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.Pageof 854