Hing AV - Search Results

1

IGF1R variants associated with isolated single suture craniosynostosis.

Cunningham ML, Horst JA, Rieder MJ, Hing AV, Stanaway IB, Park SS, Samudrala R, Speltz ML. Cunningham ML, et al. Among authors: hing av. Am J Med Genet A. 2011 Jan;155A(1):91-7. doi: 10.1002/ajmg.a.33781. Am J Med Genet A. 2011. PMID: 21204214 Free PMC article.

2

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

3

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

Hing AV, Syed N, Cunningham ML. Hing AV, et al. 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

4

MDCT diagnosis of the child with posterior plagiocephaly.

Sze RW, Hopper RA, Ghioni V, Gruss JS, Ellenbogen RG, King D, Hing AV, Cunningham ML. Sze RW, et al. Among authors: hing av. AJR Am J Roentgenol. 2005 Nov;185(5):1342-6. doi: 10.2214/AJR.04.1388. AJR Am J Roentgenol. 2005. PMID: 16247160 Review.

5

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. Among authors: hing av. 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.

6

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: hing av. Cleft Palate Craniofac J. 2006 Mar;43(2):211-21. doi: 10.1597/04-208.1. Cleft Palate Craniofac J. 2006. PMID: 16526927

7

Symbolic shape descriptors for classifying craniosynostosis deformations from skull imaging.

Lin H, Ruiz-Correa S, Shapiro LG, Hing A, Cunningham ML, Speltz M, Sze R. Lin H, et al. Conf Proc IEEE Eng Med Biol Soc. 2005;2005:6325-31. doi: 10.1109/IEMBS.2005.1615944. Conf Proc IEEE Eng Med Biol Soc. 2005. PMID: 17281714

8

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: hing av. 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

9

Syndromic craniosynostosis: from history to hydrogen bonds.

Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV. Cunningham ML, et al. Among authors: hing av. 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.

10

The morphogenesis of wormian bones: a study of craniosynostosis and purposeful cranial deformation.

Sanchez-Lara PA, Graham JM Jr, Hing AV, Lee J, Cunningham M. Sanchez-Lara PA, et al. Among authors: hing av. Am J Med Genet A. 2007 Dec 15;143A(24):3243-51. doi: 10.1002/ajmg.a.32073. Am J Med Genet A. 2007. PMID: 18000970

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