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Author/Creator Solomon, Benjamin D

3. Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. Issue 7 (11th July 2012)

Authors:
Solomon, Benjamin D; Bear, Kelly A; Wyllie, Adrian; Keaton, Amelia A; Dubourg, Christele; David, Veronique; Mercier, Sandra; Odent, Sylvie; Hehr, Ute; Paulussen, Aimee; Clegg, Nancy J; Delgado, Mauricio R; Bale, Sherri J; Lacbawan, Felicitas; Ardinger, Holly H; Aylsworth, Arthur S; Bhengu, Ntombe...
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 7(2012)
Page Start:
473
Record Type:
Journal Article
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4. Increased risk of rheumatoid arthritis among mothers with children who carry DRB1 risk-associated alleles. Issue 8 (8th April 2017)

Authors:
Cruz, Giovanna Ibeth; Shao, Xiaorong; Quach, Hong; Ho, Kimberly A; Sterba, Kirsten; Noble, Janelle A; Patsopoulos, Nikolaos A; Busch, Michael P; Triulzi, Darrell J; Wong, Wendy SW; Solomon, Benjamin D; Niederhuber, John E; Criswell, Lindsey A; Barcellos, Lisa F
Journal:
Annals of the rheumatic diseases
Issue:
Volume 76:Issue 8(2017)
Page Start:
1405
Record Type:
Journal Article
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6. Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes. Issue 12 (18th September 2015)

Authors:
Malicdan, May Christine V; Vilboux, Thierry; Stephen, Joshi; Maglic, Dino; Mian, Luhe; Konzman, Daniel; Guo, Jennifer; Yildirimli, Deniz; Bryant, Joy; Fischer, Roxanne; Zein, Wadih M; Snow, Joseph; Vemulapalli, Meghana; Mullikin, James C; Toro, Camilo; Solomon, Benjamin D; Niederhuber, John E; Ga...
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 12(2015)
Page Start:
830
Record Type:
Journal Article
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7. Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. Issue 8 (2nd December 2009)

Authors:
Solomon, Benjamin D; Lacbawan, Felicitas; Mercier, Sandra; Clegg, Nancy J; Delgado, Mauricio R; Rosenbaum, Kenneth; Dubourg, Christèle; David, Veronique; Olney, Ann Haskins; Wehner, Lars-Erik; Hehr, Ute; Bale, Sherri; Paulussen, Aimee; Smeets, Hubert J; Hardisty, Emily; Tylki-Szymanska, Anna; Pro...
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 8(2010)
Page Start:
513
Record Type:
Journal Article
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8. Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly. Issue 6 (17th April 2014)

Authors:
Bear, Kelly A; Solomon, Benjamin D; Antonini, Sonir; Arnhold, Ivo J P; França, Marcela M; Gerkes, Erica H; Grange, Dorothy K; Hadley, Donald W; Jääskeläinen, Jarmo; Paulo, Sabrina S; Rump, Patrick; Stratakis, Constantine A; Thompson, Elizabeth M; Willis, Mary; Winder, Thomas L; Jorge, Alexander A...
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 6(2014)
Page Start:
413
Record Type:
Journal Article
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