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133 results

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Page 1
Elements of morphology: standard terminology for the head and face.
Allanson JE, Cunniff C, Hoyme HE, McGaughran J, Muenke M, Neri G. Allanson JE, et al. Among authors: cunniff c. Am J Med Genet A. 2009 Jan;149A(1):6-28. doi: 10.1002/ajmg.a.32612. Am J Med Genet A. 2009. PMID: 19125436 Free PMC article.
Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance.
Powis Z, Farwell Hagman KD, Mroske C, McWalter K, Cohen JS, Colombo R, Serretti A, Fatemi A, David KL, Reynolds J, Immken L, Nagakura H, Cunniff CM, Payne K, Barbaro-Dieber T, Gripp KW, Baker L, Stamper T, Aleck KA, Jordan ES, Hersh JH, Burton J, Wentzensen IM, Guillen Sacoto MJ, Willaert R, Cho MT, Petrik I, Huether R, Tang S. Powis Z, et al. Among authors: cunniff cm. Clin Genet. 2018 Apr;93(4):752-761. doi: 10.1111/cge.13132. Epub 2018 Jan 7. Clin Genet. 2018. PMID: 28881385
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
Rieder MJ, Green GE, Park SS, Stamper BD, Gordon CT, Johnson JM, Cunniff CM, Smith JD, Emery SB, Lyonnet S, Amiel J, Holder M, Heggie AA, Bamshad MJ, Nickerson DA, Cox TC, Hing AV, Horst JA, Cunningham ML. Rieder MJ, et al. Among authors: cunniff cm. Am J Hum Genet. 2012 May 4;90(5):907-14. doi: 10.1016/j.ajhg.2012.04.002. Am J Hum Genet. 2012. PMID: 22560091 Free PMC article.
Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics.
Curry CJ, Stevenson RE, Aughton D, Byrne J, Carey JC, Cassidy S, Cunniff C, Graham JM Jr, Jones MC, Kaback MM, Moeschler J, Schaefer GB, Schwartz S, Tarleton J, Opitz J. Curry CJ, et al. Among authors: cunniff c. Am J Med Genet. 1997 Nov 12;72(4):468-77. doi: 10.1002/(sici)1096-8628(19971112)72:4<468::aid-ajmg18>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9375733 Review.
Phenotype and X inactivation in 45,X/46,X,r(X) cases.
Leppig KA, Sybert VP, Ross JL, Cunniff C, Trejo T, Raskind WH, Disteche CM. Leppig KA, et al. Among authors: cunniff c. Am J Med Genet A. 2004 Jul 30;128A(3):276-84. doi: 10.1002/ajmg.a.30002. Am J Med Genet A. 2004. PMID: 15216549
Radiological features in Brachmann-de Lange syndrome.
Braddock SR, Lachman RS, Stoppenhagen CC, Carey JC, Ireland M, Moeschler JB, Cunniff C, Graham JM Jr. Braddock SR, et al. Among authors: cunniff c. Am J Med Genet. 1993 Nov 15;47(7):1006-13. doi: 10.1002/ajmg.1320470714. Am J Med Genet. 1993. PMID: 8291513 Review.
133 results