论文信息 - Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU - 字舞流文

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

J. Stoler | C. Garel | C. Depienne | A. Toutain | C. Korff | R. Møller | A. Verloes | L. Pasquier | J. Roume | M. Parker | F. Stewart | L. Faivre | C. Le Caignec | B. Isidor | J. Andrieux | C. D. de Kovel | D. Amor | A. Rastetter | A. Bottani | E. Hirsch | V. Cormier-Daire | P. Agrawal | T. Billette de Villemeur | S. Chantot-Bastaraud | T. Attié-Bitach | S. Odent | T. Jonson | D. Heron | G. van Haaften | N. Verbeek | M. Soller | C. Mignot | M. Delrue | B. Leheup | B. Keren | F. Sheth | D. Doummar | G. VanNoy | M. Moutard | C. Alby | U. Koehler | G. Monroe | M. Vincent | C. Nava | G. Kluger | B. Koeleman | D. Pal | Pauline Marzin | S. Passemard | L. Burglen | M. V. van Haelst | A. de Saint-Martin | F. Renaldo | C. Datar | S. Scheidecker | S. Heide | C. von Stülpnagel | Lucile Boutaud | S. Naudion | C. Orzechowski | Birgit Häckl | A. De Saint-Martin | Agnès Rastetter