Chondrodysplasia punctata: A boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference47 articles.
1. Chondrodysplasia punctata with X;Y translocation
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. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
4. Chondrodystrophia calcificans congenita (Conradi's disease) in a mother and her child
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