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Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases.
Hsu WT, Shchepin DA, Mao R, Berry-Kravis E, Garber AP, Fischel-Ghodsian N, Falk RE, Carlson DE, Roeder ER, Leeth EA, Hajianpour MJ, Wang JC, Rosenblum-Vos LS, Bhatt SD, Karson EM, Hux CH, Trunca C, Bialer MG, Linn SK, Schreck RR. Hsu WT, et al. Am J Med Genet. 1998 Dec 28;80(5):473-80. doi: 10.1002/(sici)1096-8628(19981228)80:5<473::aid-ajmg7>3.0.co;2-a. Am J Med Genet. 1998. PMID: 9880211
Epilepsy in fragile X syndrome.
Berry-Kravis E. Berry-Kravis E. Dev Med Child Neurol. 2002 Nov;44(11):724-8. doi: 10.1017/s0012162201002833. Dev Med Child Neurol. 2002. PMID: 12418611
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