Article

HSPA6: s new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum.
Kause, F. ORCID: https://orcid.org/0000-0002-0074-8962, Zhang, R., Ludwig, M., Schmiedeke, E., Rissmann, A., Thiele, H., Altmueller, J. ORCID: https://orcid.org/0000-0003-4372-1521, Herms, S., Hilger, A.C., Hildebrandt, F. and Reutter, H. ORCID: https://orcid.org/0000-0002-3591-5265
Birth Defects Research 111 (10): 591-597. 1 June 2019

Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene.
Weitensteiner, V., Zhang, R., Bungenberg, J., Marks, M., Gehlen, J., Ralser, D.J., Hilger, A.C., Sharma, A., Schumacher, J., Gembruch, U., Merz, W.M., Becker, A., Altmüller, J. ORCID: https://orcid.org/0000-0003-4372-1521, Thiele, H., Herrmann, B.G., Odermatt, B., Ludwig, M. and Reutter, H. ORCID: https://orcid.org/0000-0002-3591-5265
Birth Defects Research 110 (7): 587-597. 17 April 2018