An unbalanced 46,XY,der(2)del(2)(p11.2p13) inv(2)(p11.2q13) karyotype was found in a phenotypically abnormal child with a de novo interstitial deletion of band 2p12 associated with an inv(2)(p11.2q13) inherited from the father. The inv(2) is generally considered a benign familial variant without sig
Deletion mapping and paternal origin of a Mexican AMELY negative male
✍ Scribed by J.S. Velarde-Félix; J. Salazar-Flores; G. Martínez-Cortés; A. Flores García; J.F. Muñoz-Valle; J.J. Ríos-Tostado; R. Rubi-Castellanos; H. Rangel-Villalobos
- Book ID
- 113773352
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 189 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1344-6223
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