Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene

Por Hobbs, C A, James, S J, Parsian, A, Krakowiak, P A, Jernigan, S, Greenhaw, J J, Lu, Y, Cleves, M A
Publicado em 2006

A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter.

Por Krakowiak, P A, O'Quinn, J R, Bohnsack, J F, Watkins, W S, Carey, J C, Jorde, L B, Bamshad, M
Publicado em 1997

A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.

Por Bamshad, M., Watkins, W. S., Zenger, R. K., Bohnsack, J. F., Carey, J. C., Otterud, B., Krakowiak, P. A., Robertson, M., Jorde, L. B.
Publicado em 1994

Autism-specific maternal autoantibodies recognize critical proteins in developing brain

Por Braunschweig, D, Krakowiak, P, Duncanson, P, Boyce, R, Hansen, R L, Ashwood, P, Hertz-Picciotto, I, Pessah, I N, Van de Water, J
Publicado em 2013

DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome

Por Correa-Cerro, L, Wassif, C, Waye, J, Krakowiak, P, Cozma, D, Dobson, N, Levin, S, Anadiotis, G, Steiner, R, Krajewska-Walasek, M, Nowaczyk, M, Porter, F
Publicado em 2005

Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic data.

Por Jorde, L B, Bamshad, M J, Watkins, W S, Zenger, R, Fraley, A E, Krakowiak, P A, Carpenter, K D, Soodyall, H, Jenkins, T, Rogers, A R
Publicado em 1995