A novel SHOC2 variant in Rasopathy

Por Hannig, Vickie, Jeoung, Myoungkun, Jang, Eun Ryoung, Phillips, John A., Galperin, Emilia
Publicado em 2014

What Patients and Their Relatives Think About Testing for BMPR2

Por Jones, Diana L., Sandberg, Joanne C., Rosenthal, Mary J., Saunders, Robert C., Hannig, Vickie L., Clayton, Ellen W.
Publicado em 2008

A Recurrent RNA-Splicing Mutation in the SEDL Gene Causes X-Linked Spondyloepiphyseal Dysplasia Tarda

Por Tiller, George E., Hannig, Vickie L., Dozier, Damon, Carrel, Laura, Trevarthen, Karrie C., Wilcox, William R., Mundlos, Stefan, Haines, Jonathan L., Gedeon, Agi K., Gecz, Jozef
Publicado em 2001

Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148

Por Dharmadhikari, Avinash V., Kang, Sung-Hae L., Szafranski, Przemyslaw, Person, Richard E., Sampath, Srirangan, Prakash, Siddharth K., Bader, Patricia I., Phillips, John A., Hannig, Vickie, Williams, Misti, Vinson, Sherry S., Wilfong, Angus A., Reimschisel, Tyler E., Craigen, William J., Patel, Ankita, Bi, Weimin, Lupski, James R., Belmont, John, Cheung, Sau Wai, Stankiewicz, Pawel
Publicado em 2012

A Copy Number Variation Morbidity Map of Developmental Delay

Por Cooper, Gregory M., Coe, Bradley P., Girirajan, Santhosh, Rosenfeld, Jill A., Vu, Tiffany, Baker, Carl, Williams, Charles, Stalker, Heather, Hamid, Rizwan, Hannig, Vickie, Abdel-Hamid, Hoda, Bader, Patricia, McCracken, Elizabeth, Niyazov, Dmitriy, Leppig, Kathleen, Thiese, Heidi, Hummel, Marybeth, Alexander, Nora, Gorski, Jerome, Kussmann, Jennifer, Shashi, Vandana, Johnson, Krys, Rehder, Catherine, Ballif, Blake C., Shaffer, Lisa G., Eichler, Evan E.
Publicado em 2011