Hing A - Search Results

1

Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.

Wenger TL, Dahl J, Bhoj EJ, Rosen A, McDonald-McGinn D, Zackai E, Jacobs I, Heike CL, Hing A, Santani A, Inglis AF, Sie KC, Cunningham M, Perkins J. Wenger TL, et al. Among authors: hing a. Genet Med. 2017 Jan;19(1):62-68. doi: 10.1038/gim.2016.60. Epub 2016 May 26. Genet Med. 2017. PMID: 27228464 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. Among authors: hing a. 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

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. Among authors: hing a. 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

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. 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. Among authors: hing a. 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

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

10

Syndromic craniosynostosis: from history to hydrogen bonds.

Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV. Cunningham ML, et al. 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.

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