Gastrointestinal Bleeding in the Ehlers-Danlos Syndrome

Por Beighton, Peter H.
Publicado em 1968

Hypermobility of joints

Por Beighton, Peter H., Grahame, Rodney., Bird, Howard.
Publicado em 2012

A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis

Por Gleghorn, Lindsay, Ramesar, Rajkumar, Beighton, Peter, Wallis, Gillian
Publicado em 2005

Gastrointestinal complications of the Ehlers-Danlos syndrome

Por Beighton, Peter H., Murdoch, J. Lamont, Votteler, Theodore
Publicado em 1969

Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27

Por Ianakiev, Peter, Kilpatrick, Michael W., Toudjarska, Iva, Basel, Donald, Beighton, Peter, Tsipouras, Petros
Publicado em 2000

Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2

Por Sykes, Bryan, Ogilvie, Donald, Wordsworth, Paul, Wallis, Gillian, Mathew, Chris, Beighton, Peter, Nicholls, Alan, Pope, F. Michael, Thompson, Elizabeth, Tsipouras, Petros, Schwartz, Robin, Jensson, Olafur, Arnason, Alfred, Børresen, Anne-Lise, Heiberg, Arvid, Frey, Daniel, Steinmann, Beat
Publicado em 1990

Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome

Por Kelley, Brian P, Malfait, Fransiska, Bonafe, Luisa, Baldridge, Dustin, Homan, Erica, Symoens, Sofie, Willaert, Andy, Elcioglu, Nursel, Van Maldergem, Lionel, Verellen-Dumoulin, Christine, Gillerot, Yves, Napierala, Dobrawa, Krakow, Deborah, Beighton, Peter, Superti-Furga, Andrea, De Paepe, Anne, Lee, Brendan
Publicado em 2011

Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

Por Brunkow, Mary E., Gardner, Jessica C., Van Ness, Jeff, Paeper, Bryan W., Kovacevich, Brian R., Proll, Sean, Skonier, John E., Zhao, L., Sabo, P. J., Fu, Ying-Hui, Alisch, Reid S., Gillett, Lucille, Colbert, Trenton, Tacconi, Paolo, Galas, David, Hamersma, Herman, Beighton, Peter, Mulligan, John T.
Publicado em 2001

Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

Por Reichenberger, Ernst, Tiziani, Valdenize, Watanabe, Shoji, Park, Lucy, Ueki, Yasuyoshi, Santanna, Carla, Baur, Scott T., Shiang, Rita, Grange, Dorothy K., Beighton, Peter, Gardner, Jessica, Hamersma, Herman, Sellars, Sean, Ramesar, Rajkumar, Lidral, Andrew C., Sommer, Annmarie, Raposo do Amaral, Cassio M., Gorlin, Robert J., Mulliken, John B., Olsen, Bjorn R.
Publicado em 2001

Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium

Por Farrer, Lindsay A., Grundfast, Kenneth M., Amos, Jean, Arnos, Kathleen S., Asher, James H., Beighton, Peter, Diehl, Scott R., Fex, Jörgen, Foy, Carole, Friedman, Thomas B., Greenberg, Jacquie, Hoth, Christopher, Marazita, Mary, Milunsky, Aubrey, Morell, Robert, Nance, Walter, Newton, Valerie, Ramesar, Rajkumar, Agustin, Theresa B. San, Skare, James, Stevens, Cathy A., Wagner, Ronald G., Wilcox, Edward R., Winship, Ingrid, Read, Andrew P.
Publicado em 1992