Author:
Pramyothin Pornpoj,Pithukpakorn Manop,Arakaki Richard F.
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference14 articles.
1. E.B. Hook, Prevalence, risks and recurrence, in Prenatal Diagnosis and Screening, ed. by D.J.H. Brock, C. Rodeck, M. Ferguson-Smith (Churchill Livingstone, London, 1992), pp. 351–392
2. A. Bojesen, S. Juul, C.H. Gravholt, Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J. Clin. Endocrinol. Metab. 88, 622–626 (2003)
3. C.A. Stratakis, Prader-Willi syndrome phenotype in X chromosome anomalies: evidence for a distinct syndrome. Am. J. Med. Genet. 80, 294–295 (1998)
4. M.T. Gabbett, G.B. Peters, J.M. Carmichael, A.P. Darmanian, F.A. Collins, Prader–Willi syndrome phenocopy due to duplication of Xq21.1–q21.31, with array CGH of the critical region. Clin. Genet. 73, 353–359 (2008)
5. T. Kubota, S. Nonoyama, H. Tonoki, M. Masuno, K. Imaizumi, M. Kojima, K. Wakui, M. Shimadzu, Y. Fukushima, A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR. Hum. Genet. 104, 49–55 (1999)
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