Publications by authors named "Anne V Hing"

31Publications

Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigree.

Brain 2020 Dec 22. Epub 2020 Dec 22.

Laboratory of Embryology and Genetics of Human Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR 1163, Institut Imagine, Université de Paris, 75015 Paris, France.

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December 2020

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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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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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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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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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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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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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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January 2012

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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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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January 2011

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

Plast Reconstr Surg 2009 Oct;124(4):1261-1272

Seattle, Wash. From the Department of Pediatrics, Division of Craniofacial Medicine, and the Department of Epidemiology, University of Washington and Seattle Children's Craniofacial Center.

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October 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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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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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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May 2007

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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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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November 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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August 2004