TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.
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Gao T. Wang | Mahshid S. Azamian | M. Hurles | J. Rosenfeld | L. Shaffer | P. Stankiewicz | Ankita Patel | C. Shaw | J. Lupski | S. Cheung | A. Beaudet | M. Justice | S. Leal | J. Belmont | S. Lalani | N. Katsanis | J. Hunter | C. Khor | P. Bonnen | M. York | Z. Chu | M. Hibberd | R. Omary | W. Wiszniewski | I. Campbell | C. Bacino | L. Potocki | S. Dunstan | R. Goin-Kochel | N. Hanchard | C. Simmons | Nguyen Van Vinh Chau | R. Santos-Cortez | A. Mutirangura | S. Pruthi | E. Davis | S. Boyadjiev | M. Ramocki | L. Immken | G. Scharer | P. Hixson | T. Morgan | J. Willer | P. Bader | A. Thida | K. Win | Misti D Williams | N. Madduri | A. Illner | G. Simpson | P. Yanatatsaneejit | Q. Tian | G. Zapata | Xueqing Wang | Anna Eifert | Patricia P Hernandez | Violet Gelowani | M. Maletić-Savatić | Heather P Crawford | Lisa Omo-Griffith | A. A. Franklin | A. Ester | Jeffery Kerr | Muhammad Haque | Marija Stosic | T. E. Gallagher | M. Williams | Heather P. Crawford
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