Publications by authors named "Anne Hing"

37Publications

Clinical characteristics and surgical decision making for infants with metopic craniosynostosis in conjunction with other congenital anomalies.

Plast Reconstr Surg Glob Open 2013 Oct 7;1(7):e62. Epub 2013 Nov 7.

Department of Surgery/Division of Plastic Surgery, University of Washington, Seattle, Wash.; and the Department of Pediatrics and Craniofacial Center, Seattle Children's Hospital, Seattle, Wash.

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http://dx.doi.org/10.1097/GOX.0b013e3182a87e9bDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174064PMC
October 2013

Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.

Am J Hum Genet 2014 Aug;95(2):235-40

Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA; Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Craniofacial Center, Seattle Children's Hospital, Seattle, WA 98105, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.07.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129399PMC
August 2014

Oculoauriculofrontonasal syndrome: case series revealing new bony nasal anomalies in an old syndrome.

Am J Med Genet A 2013 Jun 1;161A(6):1345-53. Epub 2013 May 1.

Department of Pediatrics, University of Washington, Seattle Children's Craniofacial Center, Seattle, Washington 98105, USA.

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http://dx.doi.org/10.1002/ajmg.a.35926DOI Listing
June 2013

Making the diagnosis: metopic ridge versus metopic craniosynostosis.

J Craniofac Surg 2013 Jan;24(1):178-85

From the University of Washington and Seattle Children's Hospital, Seattle, WA 98105, USA.

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http://dx.doi.org/10.1097/SCS.0b013e31826683d1DOI Listing
January 2013

Evaluation of ICD-9-CM codes for craniofacial microsomia.

Birth Defects Res A Clin Mol Teratol 2012 Dec 18;94(12):990-5. Epub 2012 Aug 18.

Seattle Children's Hospital, Craniofacial Center, Seattle, Washington 98101, USA.

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http://dx.doi.org/10.1002/bdra.23059DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522759PMC
December 2012

New developments in genetic diagnosis: implications for the craniofacial surgeon.

J Craniofac Surg 2012 Jan;23(1):212-6

University of Washington, Seattle Children's Hospital, Seattle, Washington 98105, USA.

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http://dx.doi.org/10.1097/SCS.0b013e318241ae88DOI Listing
January 2012

Microtia: epidemiology and genetics.

Am J Med Genet A 2012 Jan 21;158A(1):124-39. Epub 2011 Nov 21.

Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA.

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http://doi.wiley.com/10.1002/ajmg.a.34352
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http://dx.doi.org/10.1002/ajmg.a.34352DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482263PMC
January 2012

Bathrocephaly: a head shape associated with a persistent mendosal suture.

Cleft Palate Craniofac J 2013 Jan 4;50(1):104-8. Epub 2011 Oct 4.

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http://journals.sagepub.com/doi/10.1597/11-153
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http://dx.doi.org/10.1597/11-153DOI Listing
January 2013

Robin sequence: from diagnosis to development of an effective management plan.

Pediatrics 2011 May 4;127(5):936-48. Epub 2011 Apr 4.

Children's Craniofacial Center, Seattle Children's Hospital, Box 5371, M/S W7847, Seattle, WA 98145, USA.

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http://dx.doi.org/10.1542/peds.2010-2615DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387866PMC
May 2011

IGF1R variants associated with isolated single suture craniosynostosis.

Am J Med Genet A 2011 Jan;155A(1):91-7

Seattle Children's Hospital Craniofacial Center, University of Washington, 98195, USA.

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http://dx.doi.org/10.1002/ajmg.a.33781DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3059230PMC
January 2011

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

Plast Reconstr Surg 2009 Oct;124(4):1261-72

Department of Pediatrics, Division of Craniofacial Medicine, University of Washington and Seattle Children's Hospital, Seattle, Wash. 98105-5371, USA.

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http://dx.doi.org/10.1097/PRS.0b013e3181b454bdDOI Listing
October 2009

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

Am J Med Genet A 2009 May;149A(5):1024-32

Department of Pediatrics, University of Washington, Seattle, Washington 98195-6320, USA.

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http://dx.doi.org/10.1002/ajmg.a.32782DOI Listing
May 2009

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

Am J Med Genet A 2007 Dec;143A(24):3243-51

Medical Genetics Institute, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

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http://dx.doi.org/10.1002/ajmg.a.32073DOI Listing
December 2007

Syndromic craniosynostosis: from history to hydrogen bonds.

Orthod Craniofac Res 2007 May;10(2):67-81

Division of Craniofacial Medicine, University of Washington Department of Pediatrics and Children's Craniofacial Center, Children's Hospital and Regional Medical Center, Seattle, WA, USA.

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http://dx.doi.org/10.1111/j.1601-6343.2007.00389.xDOI Listing
May 2007

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

Cleft Palate Craniofac J 2007 May;44(3):340-6

Department of Pediatrics, Division of Craniofacial Medicine, University of Washington and Children's Hospital and Regional Medical Center, Seattle, Washington, USA.

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http://dx.doi.org/10.1597/05-196DOI Listing
May 2007

Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.

Am J Med Genet A 2007 Apr;143A(7):678-86

Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195-6320, USA.

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http://dx.doi.org/10.1002/ajmg.a.31630DOI Listing
April 2007

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

Cleft Palate Craniofac J 2006 Mar;43(2):211-21

Department of Radiology, University of Washington, Seattle, WA 98105, USA.

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http://dx.doi.org/10.1597/04-208.1DOI Listing
March 2006

A novel oculo-oto-facial dysplasia in a Native Alaskan community with autosomal recessive inheritance.

Am J Med Genet A 2006 Apr;140(8):804-12

Department of Pediatrics, University of Washington, Seattle, Washington, USA.

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http://dx.doi.org/10.1002/ajmg.a.31160DOI Listing
April 2006

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

Birth Defects Res A Clin Mol Teratol 2006 Feb;76(2):78-85

Children's Craniofacial Center, Children's Hospital and Regional Medical Center, Seattle, Washington 98195-6320, USA.

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http://doi.wiley.com/10.1002/bdra.20231
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http://dx.doi.org/10.1002/bdra.20231DOI Listing
February 2006

MDCT diagnosis of the child with posterior plagiocephaly.

AJR Am J Roentgenol 2005 Nov;185(5):1342-6

Department of Radiology, University of Washington, 4800 Sand Point Way NE, PO Box 5371/CH-69, Seattle, WA 98105-0371, USA.

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http://dx.doi.org/10.2214/AJR.04.1388DOI Listing
November 2005

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

Am J Med Genet A 2005 May;135(1):13-20

Department of Pediatrics, Division of Genetics, University of California-San Francisco, 553 Parnassus Street, Rm. U-585P, San Francisco, CA 94143, USA.

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http://dx.doi.org/10.1002/ajmg.a.30694DOI Listing
May 2005

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

Am J Med Genet A 2004 Aug;128A(4):374-82

Division of Genetics and Development, Department of Pediatrics, University of Washington, Seattle, Washington 98195-6320, USA.

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http://doi.wiley.com/10.1002/ajmg.a.30091
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http://dx.doi.org/10.1002/ajmg.a.30091DOI Listing
August 2004