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Heterogeneity of Chondrodysplasia punctata
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Most cited references33
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Familial Neurovisceral Lipidosis: An Analysis of Eight Cases of a Syndrome Previously Reported as "Hurler-Variant," "Pseudo-Hurler Disease," and "Tay-Sachs Disease With Visceral Involvement"
BENJAMIN H. LANDING (1964)
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Follicular Atrophoderma and Pseudopelade Associated with Chondrodystrophia Calcificans Congenita**From the Department of Dermatology, College of Physicians and Surgeons, Columbia University, and the Vanderbilt Clinic.
Helen Curth (1949)