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Journal of Psychiatric Research|April 24, 2017
The dimensional structure of psychopathology in 22q11.2 Deletion SyndromeMaria Niarchou, Tyler M Moore, Sunny X Tang, et al.Human Molecular Genetics|March 1, 1995
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndromeU Schell, A Hehr, G J Feldman, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 26, 2006
Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutationsSuzanne K Jadico, David A Young, Alexandra Huebner, et al.The Journal of Thoracic and Cardiovascular Surgery|January 9, 2008
Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of FallotIlana Zeltser, Gail P Jarvik, Judy Bernbaum, et al.The Journal of Pediatrics|February 5, 1999
Psychoeducational profile of the 22q11.2 microdeletion: A complex patternE M Moss, M L Batshaw, C B Solot, et al.The Journal of Pediatrics|May 15, 1998
Identification of a genetic cause for isolated unilateral coronal synostosis: a unique mutation in the fibroblast growth factor receptor 3K W Gripp, D M McDonald-McGinn, K Gaudenz, et al.American Journal of Human Genetics|April 1, 1995
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6G J Feldman, N H Robin, L A Brueton, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndromeShin-Ichi Horike, Jose Carlos P Ferreira, Makiko Meguro-Horike, et al.Annals of Plastic Surgery|July 9, 2014
A 35-year experience with syndromic cleft palate repair: operative outcomes and long-term speech functionMarten N Basta, Jason Silvestre, Carrie Stransky, et al.American Journal of Medical Genetics. Part A|December 28, 2020
Cardiac evaluation of patients with 22q11.2 duplication syndromeAdam Butensky, Chiara Pandolfi de Rinaldis, Shrey Patel, et al.Pageof 63