MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development

An essential and highly conserved role for Zic3 in left–right patterning, gastrulation and convergent extension morphogenesis

(2012) Ashley E. Cast et al.   DEVELOPMENTAL BIOLOGY

Transcription factor COUP-TFII is indispensable for venous and lymphatic development in zebrafish and Xenopus laevis

(2011) Xabier L. Aranguren et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis

(2011) Sumito Dateki et al.   ENDOCRINE JOURNAL

Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans

(2010) Bernard Thienpont et al.   AMERICAN JOURNAL OF HUMAN GENETICS

5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects

(2010) Eiki Nakamura et al.   European Journal of Medical Genetics

Clinical and Functional Characteristics of a Novel Heterozygous Mutation of theIGF1RGene and IGF1R Haploinsufficiency due to Terminal 15q26.2->qter Deletion in Patients with Intrauterine Growth Retardation and Postnatal Catch-Up Growth Failure

(2010) Jin-Ho Choi et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort

(2008) Julia Baptista et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay

(2008) Josef Davidsson et al.   BMC Medical Genetics

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

(2008) K. L. McBride et al.   HUMAN MOLECULAR GENETICS