XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome)
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference25 articles.
1. Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation
2. X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene
3. Chondrodystrophia calcificans congenita (Conradi's disease) in a mother and her child
4. (1901): “Die Nervenverteilung in der Haut in ihrer Beziehung zu den Erkrankungen der Haut.” Wien and Leipzig: Braumullcr.
5. Expression of the Gene Defect in X-Linked Agammaglobulinemia
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