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Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

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Title: Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
Authors: Li, Feng1,2, Shen, Yiping3, Köhler, Udo4, Sharkey, Freddie H.5, Menon, Deepa6, Coulleaux, Laurence7, Malan, Valérie7, Rio, Marlène7, McMullan, Dominic J.8, Cox, H.9, Fagan, Kerry A.10, Gaunt, Lorraine11, Metcalfe, Kay11, Heinrich, Uwe12, Hislop, Gordon13, Maye, Una14, Sutcliffe, Maxine15, Wu, Bai-Lin3, Thiel, Brian D.16, Mulchandani, Surabhi16
Source: European Journal of Medical Genetics. Mar2010, Vol. 53 Issue 2, p93-99. 7p.
Database: Academic Search Ultimate
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  Data: Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
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  Data: <searchLink fieldCode="AR" term="%22Li%2C+Feng%22">Li, Feng</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Shen%2C+Yiping%22">Shen, Yiping</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Köhler%2C+Udo%22">Köhler, Udo</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Sharkey%2C+Freddie+H%2E%22">Sharkey, Freddie H.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Menon%2C+Deepa%22">Menon, Deepa</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Coulleaux%2C+Laurence%22">Coulleaux, Laurence</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Malan%2C+Valérie%22">Malan, Valérie</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Rio%2C+Marlène%22">Rio, Marlène</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22McMullan%2C+Dominic+J%2E%22">McMullan, Dominic J.</searchLink><relatesTo>8</relatesTo><br /><searchLink fieldCode="AR" term="%22Cox%2C+H%2E%22">Cox, H.</searchLink><relatesTo>9</relatesTo><br /><searchLink fieldCode="AR" term="%22Fagan%2C+Kerry+A%2E%22">Fagan, Kerry A.</searchLink><relatesTo>10</relatesTo><br /><searchLink fieldCode="AR" term="%22Gaunt%2C+Lorraine%22">Gaunt, Lorraine</searchLink><relatesTo>11</relatesTo><br /><searchLink fieldCode="AR" term="%22Metcalfe%2C+Kay%22">Metcalfe, Kay</searchLink><relatesTo>11</relatesTo><br /><searchLink fieldCode="AR" term="%22Heinrich%2C+Uwe%22">Heinrich, Uwe</searchLink><relatesTo>12</relatesTo><br /><searchLink fieldCode="AR" term="%22Hislop%2C+Gordon%22">Hislop, Gordon</searchLink><relatesTo>13</relatesTo><br /><searchLink fieldCode="AR" term="%22Maye%2C+Una%22">Maye, Una</searchLink><relatesTo>14</relatesTo><br /><searchLink fieldCode="AR" term="%22Sutcliffe%2C+Maxine%22">Sutcliffe, Maxine</searchLink><relatesTo>15</relatesTo><br /><searchLink fieldCode="AR" term="%22Wu%2C+Bai-Lin%22">Wu, Bai-Lin</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Thiel%2C+Brian+D%2E%22">Thiel, Brian D.</searchLink><relatesTo>16</relatesTo><br /><searchLink fieldCode="AR" term="%22Mulchandani%2C+Surabhi%22">Mulchandani, Surabhi</searchLink><relatesTo>16</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Medical+Genetics%22">European Journal of Medical Genetics</searchLink>. Mar2010, Vol. 53 Issue 2, p93-99. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=50227445
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