W e describe a newborn with a novel interstitial deletion of the long arm of chromosome 17 [del (17) (q23.2q24.3)I who died on day of life 17 during a recurrent apneic episode. Her phenotype included severe growth retardation, multiple facial anomalies, maldeveloped oralpharyngeal structures, and di
Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies
β Scribed by Zenger-Hain, Julie L. ;Roberson, Jacquelyn ;Van Dyke, Daniel L. ;Weiss, Lester
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 246 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0148-7299
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