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Identification of DNA recognition sequences for the Pax3 paired domain

✍ Scribed by Georges Chalepakis; Peter Gruss


Book ID
116132916
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
439 KB
Volume
162
Category
Article
ISSN
0378-1119

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## Semmzu Craniofacial-deafnesshand syndrome (MIM 122880) is inherited as an autosomal dominant mutation characterized by the absence or hypoplasia of the nasal bones, profound sensorineural deafness, a small and short nose with slitlike nares, hypertelorism, short palpebral fissures, and limited