Cunningham ML - Search Results

1

Haploinsufficiency of SF3B2 causes craniofacial microsomia.

Timberlake AT, Griffin C, Heike CL, Hing AV, Cunningham ML, Chitayat D, Davis MR, Doust SJ, Drake AF, Duenas-Roque MM, Goldblatt J, Gustafson JA, Hurtado-Villa P, Johns A, Karp N, Laing NG, Magee L; University of Washington Center for Mendelian Genomics; Mullegama SV, Pachajoa H, Porras-Hurtado GL, Schnur RE, Slee J, Singer SL, Staffenberg DA, Timms AE, Wise CA, Zarante I, Saint-Jeannet JP, Luquetti DV. Timberlake AT, et al. Among authors: cunningham ml. Nat Commun. 2021 Aug 3;12(1):4680. doi: 10.1038/s41467-021-24852-9. Nat Commun. 2021. PMID: 34344887 Free PMC article.

2

Familial acromelic frontonasal dysostosis: autosomal dominant inheritance with reduced penetrance.

Hing AV, Syed N, Cunningham ML. Hing AV, et al. Among authors: cunningham ml. Am J Med Genet A. 2004 Aug 1;128A(4):374-82. doi: 10.1002/ajmg.a.30091. Am J Med Genet A. 2004. PMID: 15264282

3

Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?

Heike CL, Cunningham ML, Steiner RD, Wenkert D, Hornung RL, Gruss JS, Gannon FH, McAlister WH, Mumm S, Whyte MP. Heike CL, et al. Among authors: cunningham ml. Am J Med Genet A. 2005 Dec 1;139A(2):67-77. doi: 10.1002/ajmg.a.30915. Am J Med Genet A. 2005. PMID: 16222671

4

Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations.

Cunningham ML, Seto ML, Hing AV, Bull MJ, Hopkin RJ, Leppig KA. Cunningham ML, et al. Birth Defects Res A Clin Mol Teratol. 2006 Feb;76(2):78-85. doi: 10.1002/bdra.20231. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16463420 Review.

5

New scaphocephaly severity indices of sagittal craniosynostosis: a comparative study with cranial index quantifications.

Ruiz-Correa S, Sze RW, Starr JR, Lin HT, Speltz ML, Cunningham ML, Hing AV. Ruiz-Correa S, et al. Among authors: cunningham ml. Cleft Palate Craniofac J. 2006 Mar;43(2):211-21. doi: 10.1597/04-208.1. Cleft Palate Craniofac J. 2006. PMID: 16526927

6

Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.

Seto ML, Hing AV, Chang J, Hu M, Kapp-Simon KA, Patel PK, Burton BK, Kane AA, Smyth MD, Hopper R, Ellenbogen RG, Stevenson K, Speltz ML, Cunningham ML. Seto ML, et al. Among authors: cunningham ml. Am J Med Genet A. 2007 Apr 1;143A(7):678-86. doi: 10.1002/ajmg.a.31630. Am J Med Genet A. 2007. PMID: 17343269

7

Evaluation of the infant with an abnormal skull shape.

Cunningham ML, Heike CL. Cunningham ML, et al. Curr Opin Pediatr. 2007 Dec;19(6):645-51. doi: 10.1097/MOP.0b013e3282f1581a. Curr Opin Pediatr. 2007. PMID: 18025930 Review.

8

Bilateral lambdoid and sagittal synostosis (BLSS): a unique craniosynostosis syndrome or predictable craniofacial phenotype?

Hing AV, Click ES, Holder U, Seto ML, Vessey K, Gruss J, Hopper R, Cunningham ML. Hing AV, et al. Among authors: cunningham ml. Am J Med Genet A. 2009 May;149A(5):1024-32. doi: 10.1002/ajmg.a.32782. Am J Med Genet A. 2009. PMID: 19396832 Review.

9

Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome.

Heike CL, Starr JR, Rieder MJ, Cunningham ML, Edwards KL, Stanaway IB, Crawford DC. Heike CL, et al. Among authors: cunningham ml. Birth Defects Res A Clin Mol Teratol. 2010 Jan;88(1):54-63. doi: 10.1002/bdra.20604. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 19645056 Free PMC article.

10

Picture perfect? Reliability of craniofacial anthropometry using three-dimensional digital stereophotogrammetry.

Heike CL, Cunningham ML, Hing AV, Stuhaug E, Starr JR. Heike CL, et al. Among authors: cunningham ml. Plast Reconstr Surg. 2009 Oct;124(4):1261-1272. doi: 10.1097/PRS.0b013e3181b454bd. Plast Reconstr Surg. 2009. PMID: 19935311

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