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Genotype and phenotype in Angelman syndrome caused by paternal UPD 15

✍ Scribed by Prasad, Chitra; Wagstaff, Joseph


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
195 KB
Volume
70
Category
Article
ISSN
0148-7299

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## Abstract Du Pan syndrome is a rare acromesomelic dysplasia with characteristic clinical and radiographic findings. It is inherited as an autosomal recessive trait. Almost all the patients reported have been from Muslim countries. We report on a female and her child with Du Pan syndrome from a Ca