Structural Changes in Chromosomes
Author:
Publisher
Springer India
Link
http://link.springer.com/content/pdf/10.1007/978-81-322-3673-3_12
Reference12 articles.
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4. Giordano M, Gertosio C, Pagani S, Meazza C, Fusco I, Bozzola E, Bozzola M (2015) A 5.8 Mb interstitial deletion on chromosome Xq21.1 in a boy with intellectual disability, cleft palate, hearing impairment and combined growth hormone deficiency. BMC Med Genet 16:74. doi: 10.1186/s12881-015-0220-z
5. Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, Itsara A, Vives L, Walsh T, McCarthy SE, Baker C, Mefford HC, Kidd JM, Browning SR, Browning BL, Dickel DE, Levy DL, Ballkif BC, Platky K, Farber DM, Gowans GC, Wetherbee JJ, Asamoah A, Weaver DD, Mark PR, Dickerson J et al (2010) A recurrent 16p12.1 microdeletion supports a two hit model for severe developmental delay. Nat Genet 42:203–209
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