Brian C. Schutte

发表

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

K. Christensen, B. Maher, M. Marazita, 2004, The New England journal of medicine.

Abnormal brain structure in adults with Van der Woude syndrome

N. Andreasen, P. Nopoulos, J. Murray, 2007, Clinical genetics.

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

J C Murray, R Pfundt, R. Pfundt, 2007, Journal of Medical Genetics.

A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

S. Gregory, B. Bjork, J. Murray, 2000, Genome research.

Variable airway responsiveness to inhaled lipopolysaccharide.

D. Schwartz, G. Hunninghake, L. Powers, 1999, American journal of respiratory and critical care medicine.

Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding tudor and KH domains.

I. Marenholz, D. Mischke, B. Schutte, 2000, Gene.

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

S. Patil, B. Bjork, J. Murray, 1999, American journal of medical genetics.

Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.

J. Murray, B. Schutte, A. Sander, 1996, Genomics.

Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

V. Sheffield, R. Carmi, D. Landau, 1998, American journal of human genetics.

Thyroid hormone regulation of the NADH shuttles in liver and cardiac mitochondria.

T. Scholz, B. Schutte, C. Teneyck, 2000, Journal of molecular and cellular cardiology.