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Translational Psychiatry|July 5, 2017
Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated childrenI Gozes, A Van Dijck, G Hacohen-Kleiman, et al.
Translational Psychiatry|February 22, 2017
Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated childrenI Gozes, A Van Dijck, G Hacohen-Kleiman, et al.
Clinical Genetics|February 3, 2006
Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnosticsL Rooms, E Reyniers, W Wuyts, et al.
American Journal of Human Genetics|January 13, 2000
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)E Holinski-Feder, E Reyniers, S Uhrig, et al.
Human Molecular Genetics|June 13, 1998
L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsE Fransen, R D'Hooge, G Van Camp, et al.
Annals of Human Genetics|November 1, 1996
European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme HumainS A Cox, J Attwood, S P Bryant, et al.
Molecular Psychiatry|June 1, 2016
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypesM N Loviglio, M Leleu, K Männik, et al.
Nature|February 5, 2010
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2R G Walters, S Jacquemont, A Valsesia, et al.
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