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Clinical Dysmorphology|October 1, 1994
De la Chapelle dysplasia (atelosteogenesis type II): case report and review of the literature [corrected]C Schrander-Stumpel, M Havenith, E V Linden, et al.Clinical Dysmorphology|July 1, 1995
Ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosumH M Saal, D I BulasClinical Dysmorphology|January 1, 1994
A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parentsL I al Gazali, K Sabrinathan, K G NairClinical Dysmorphology|January 1, 1994
An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like featuresA A Schinzel, W P Robinson, F Binkert, et al.Clinical Dysmorphology|October 1, 1995
Absent iris stroma, narrow body build and small facial bones: a new association or variant of SHORT syndrome?A Bankier, C G Keith, I K TempleClinical Dysmorphology|October 1, 1995
A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?P D Turnpenny, D C De Silva, D W Gregory, et al.Clinical Dysmorphology|January 1, 1996
The microcephaly-lymphoedema syndrome: report of an additional familyC Kozma, N Scribanu, E GershClinical Dysmorphology|January 1, 1996
Are cardio-facio-cutaneous syndrome and Noonan syndrome distinct? A case of CFC offspring of a mother with Noonan syndromeL G LeichtmanPageof 117