Heike CL - 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: heike cl. Nat Commun. 2021 Aug 3;12(1):4680. doi: 10.1038/s41467-021-24852-9. Nat Commun. 2021. PMID: 34344887 Free PMC article.

2

Observations by Caregivers Using the Infant with Clefts Observation Outcomes Instrument (iCOO): A Comparison of Three Versus Seven-day Daily Diaries.

Rahman M, Leroux BG, McKinney CM, Kapp-Simon KA, Edwards T, Jones SM, Rosenberg JM, Patrick D, Daniels K, Stueckle L, Heike CL. Rahman M, et al. Among authors: heike cl. Cleft Palate Craniofac J. 2023 May 15:10556656231175290. doi: 10.1177/10556656231175290. Online ahead of print. Cleft Palate Craniofac J. 2023. PMID: 37186767

3

Century of Jackson-Weiss syndrome: further definition of clinical and radiographic findings in "lost" descendants of the original kindred.

Heike C, Seto M, Hing A, Palidin A, Hu FZ, Preston RA, Ehrlich GD, Cunningham M. Heike C, et al. Am J Med Genet. 2001 May 15;100(4):315-24. doi: 10.1002/ajmg.1266. Am J Med Genet. 2001. PMID: 11343323

4

Craniofacial defects of blastogenesis: duplication of pituitary with cleft palate and orophgaryngeal tumors.

Slavotinek A, Parisi M, Heike C, Hing A, Huang E. Slavotinek A, et al. Am J Med Genet A. 2005 May 15;135(1):13-20. doi: 10.1002/ajmg.a.30694. Am J Med Genet A. 2005. PMID: 15810008 Review.

5

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. 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

6

Sleep disturbances in 22q11.2 deletion syndrome: a case with obstructive and central sleep apnea.

Heike CL, Avellino AM, Mirza SK, Kifle Y, Perkins J, Sze R, Egbert M, Hing AV. Heike CL, et al. Cleft Palate Craniofac J. 2007 May;44(3):340-6. doi: 10.1597/05-196. Cleft Palate Craniofac J. 2007. PMID: 17477750

7

Syndromic craniosynostosis: from history to hydrogen bonds.

Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV. Cunningham ML, et al. Among authors: heike cl. Orthod Craniofac Res. 2007 May;10(2):67-81. doi: 10.1111/j.1601-6343.2007.00389.x. Orthod Craniofac Res. 2007. PMID: 17552943 Review.

8

Evaluation of the infant with an abnormal skull shape.

Cunningham ML, Heike CL. Cunningham ML, et al. Among authors: heike cl. Curr Opin Pediatr. 2007 Dec;19(6):645-51. doi: 10.1097/MOP.0b013e3282f1581a. Curr Opin Pediatr. 2007. PMID: 18025930 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. 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. Plast Reconstr Surg. 2009 Oct;124(4):1261-1272. doi: 10.1097/PRS.0b013e3181b454bd. Plast Reconstr Surg. 2009. PMID: 19935311

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