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1 Ergebnisse
1
Correction to: De novo and inherited TCF20 pathogenic varia..:
The DDD study
;
Vetrini, Francesco
;
McKee, Shane
...
Genome Medicine. 11 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/s13073-019-0630-1
RT Journal T1
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13073-019-0630-1&Exemplar=1&LAN=DE A1 The DDD study A1 Vetrini, Francesco A1 McKee, Shane A1 Rosenfeld, Jill A. A1 Suri, Mohnish A1 Lewis, Andrea M. A1 Nugent, Kimberly Margaret A1 Roeder, Elizabeth A1 Littlejohn, Rebecca O. A1 Holder, Sue A1 Zhu, Wenmiao A1 Alaimo, Joseph T. A1 Graham, Brett A1 Harris, Jill M. A1 Gibson, James B. A1 Pastore, Matthew A1 McBride, Kim L. A1 Komara, Makanko A1 Al-Gazali, Lihadh A1 Al Shamsi, Aisha A1 Fanning, Elizabeth A. A1 Wierenga, Klaas J. A1 Scott, Daryl A. A1 Ben-Neriah, Ziva A1 Meiner, Vardiella A1 Cassuto, Hanoch A1 Elpeleg, Orly A1 Lloyd Holder Jr, J. A1 Burrage, Lindsay C. A1 Seaver, Laurie H. PB Springer Science and Business Media LLC YR 2019 SN 1756-994X JF Genome Medicine VO 11 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13073-019-0630-1 DO https://doi.org/10.1186/s13073-019-0630-1 SF ELIB - SuUB Bremen
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