Thymidylate Synthetase in Mutants of DROSOPHILA MELANOGASTER

Por Carpenter, Nancy J.
Publicado em 1973

A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Determine the Effect of Romiplostim on Health‐Related Quality of Life in Children with Primary Immune Thrombocytope...

Por Mathias, Susan D., Li, Xiaoyan, Eisen, Melissa, Carpenter, Nancy, Crosby, Ross D., Blanchette, Victor S.
Publicado no Pediatr Blood Cancer (2016)

PRELIMINARY COMMUNICATION: PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE X SYNDROME

Por Butler, Merlin G., Allen, G. Andy, Singh, Dharmdeo N., Carpenter, Nancy J., Hall, Bryan D.
Publicado no Am J Med Genet (1988)

Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene

Por Schwartz, Charles E. , May, Melanie M. , Carpenter, Nancy J. , Rogers, R. Curtis , Martin, Judith , Bialer, Martin G. , Ward, Jewell , Sanabria, Javier , Marsa, Silvana , Lewis, James A. , Echeverri, Roberto , Lubs, Herbert A. , Voeller, Kytja , Simensen, Richard J. , Stevenson, Roger E. 
Publicado em 2005

Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population

Por Crawford, Dana C., Schwartz, Charles E., Meadows, Kellen L., Newman, James L., Taft, Lisa F., Gunter, Chris, Brown, W. Ted, Carpenter, Nancy J., Howard-Peebles, Patricia N., Monaghan, Kristin G., Nolin, Sarah L., Reiss, Allan L., Feldman, Gerald L., Rohlfs, Elizabeth M., Warren, Stephen T., Sherman, Stephanie L.
Publicado em 2000

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

Por Korbel, Jan O., Tirosh-Wagner, Tal, Urban, Alexander Eckehart, Chen, Xiao-Ning, Kasowski, Maya, Dai, Li, Grubert, Fabian, Erdman, Chandra, Gao, Michael C., Lange, Ken, Sobel, Eric M., Barlow, Gillian M., Aylsworth, Arthur S., Carpenter, Nancy J., Clark, Robin Dawn, Cohen, Monika Y., Doran, Eric, Falik-Zaccai, Tzipora, Lewin, Susan O., Lott, Ira T., McGillivray, Barbara C., Moeschler, John B., Pettenati, Mark J., Pueschel, Siegfried M., Rao, Kathleen W., Shaffer, Lisa G., Shohat, Mordechai, Van Riper, Alexander J., Warburton, Dorothy, Weissman, Sherman, Gerstein, Mark B., Snyder, Michael, Korenberg, Julie R.
Publicado em 2009

Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation

Por Tarpey, Patrick S. , Stevens, Claire , Teague, Jon , Edkins, Sarah , O’Meara, Sarah , Avis, Tim , Barthorpe, Syd , Buck, Gemma , Butler, Adam , Cole, Jennifer , Dicks, Ed , Gray, Kristian , Halliday, Kelly , Harrison, Rachel , Hills, Katy , Hinton, Jonathon , Jones, David , Menzies, Andrew , Mironenko, Tatiana , Perry, Janet , Raine, Keiran , Richardson, David , Shepherd, Rebecca , Small, Alexandra , Tofts, Calli , Varian, Jennifer , West, Sofie , Widaa, Sara , Yates, Andy , Catford, Rachael , Butler, Julia , Mallya, Uma , Moon, Jenny , Luo, Ying , Dorkins, Huw , Thompson, Deborah , Easton, Douglas F. , Wooster, Richard , Bobrow, Martin , Carpenter, Nancy , Simensen, Richard J. , Schwartz, Charles E. , Stevenson, Roger E. , Turner, Gillian , Partington, Michael , Gecz, Jozef , Stratton, Michael R. , Futreal, P. Andrew , Raymond, F. Lucy 
Publicado em 2006