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Cytogenetic and Genome Research|March 22, 2012
Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literatureA L Berner, S Bağci, E Wohlleber, et al.Cytogenetic and Genome Research|June 29, 2011
De novo partial trisomy 18p and partial monosomy 18q in a patient with anorectal malformationE Bartels, M Draaken, B Kazmierczak, et al.Clinical Genetics|December 16, 2016
Mutations in CRLF1 cause familial achalasiaA Busch, M Žarković, C Lowe, et al.Klinische Padiatrie|August 24, 2012
A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRLS M Pasternack, D Böckenhauer, M Refke, et al.The Journal of Urology|February 26, 2008
Epidemiological survey of 214 families with bladder exstrophy-epispadias complexL Gambhir, T Höller, M Müller, et al.Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.Pediatric Surgery International|September 25, 2012
Practice of dilatation after surgical correction in anorectal malformationsEkkehart Jenetzky, S Reckin, E Schmiedeke, et al.Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|November 7, 2015
Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German familiesN Zwink, V Choinitzki, F Baudisch, et al.Journal of Dental Research|February 25, 2014
Strong association of variants around FOXE1 and orofacial cleftingK U Ludwig, A C Böhmer, M Rubini, et al.Journal of Dental Research|August 3, 2017
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome SequencingA K Hoebel, D Drichel, M van de Vorst, et al.Pageof 3