Anne V Hing
Geneticist | Clinical Genetics (M.D.)
4800 Sand Point Way Ne Seattle WA, 98105About
Anne V. Hing, MD, is attending physician at Seattle Childrens Hospital, associate professor in the Department of Pediatrics at the University of Washington School of Medicine and adjunct faculty member ...
Education and Training
Washington Center / School of Medicine 1985
Washington University in St. Louis School of Medicine 1985
Provider Details
Expert Publications
Data provided by the National Library of Medicine- GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease.
- Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and pro alpha 2 (I) collagen (COL1A2).
- Familial acromelic frontonasal dysostosis: autosomal dominant inheritance with reduced penetrance.
- MDCT diagnosis of the child with posterior plagiocephaly.
- New scaphocephaly severity indices of sagittal craniosynostosis: a comparative study with cranial index quantifications.
- Sleep disturbances in 22q11.2 deletion syndrome: a case with obstructive and central sleep apnea.
- Syndromic craniosynostosis: from history to hydrogen bonds.
- The morphogenesis of wormian bones: a study of craniosynostosis and purposeful cranial deformation.
- Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
- Bilateral lambdoid and sagittal synostosis (BLSS): a unique craniosynostosis syndrome or predictable craniofacial phenotype?
- IGF1R variants associated with isolated single suture craniosynostosis.
- Robin sequence: from diagnosis to development of an effective management plan.
- Bathrocephaly: a head shape associated with a persistent mendosal suture.
- Oculoauriculofrontonasal syndrome: case series revealing new bony nasal anomalies in an old syndrome.
- Clinical characteristics and surgical decision making for infants with metopic craniosynostosis in conjunction with other congenital anomalies.
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