Publications by authors named "Chin-To Fong"

27Publications

A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia.

HeartRhythm Case Rep 2016 Jan 13;2(1):32-35. Epub 2015 Oct 13.

University of Rochester School of Medicine and Dentistry, Department of Pediatrics, Division of Pediatric Cardiology.

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http://dx.doi.org/10.1016/j.hrcr.2015.08.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412637PMC
January 2016

A culinary laboratory for nutrition education.

Clin Teach 2016 Jun 25;13(3):197-201. Epub 2015 Jun 25.

Department of Pediatrics, University of Rochester, New York, USA.

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http://dx.doi.org/10.1111/tct.12403DOI Listing
June 2016

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.

JAMA 2014 Aug;312(7):729-38

Department of Pediatrics, University of California, San Francisco, San Francisco2UCSF Benioff Children's Hospital, San Francisco, California.

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http://primaryimmune.org/wp-content/uploads/2014/10/August-2
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http://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabl
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http://jama.jamanetwork.com/article.aspx?doi=10.1001/jama.20
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http://dx.doi.org/10.1001/jama.2014.9132DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492158PMC
August 2014

Sapropterin dihydrochloride use in pregnant women with phenylketonuria: an interim report of the PKU MOMS sub-registry.

Mol Genet Metab 2014 May 12;112(1):9-16. Epub 2014 Mar 12.

BioMarin Pharmaceutical Inc., 105 Digital Drive, Novato, CA 94949, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2014.02.016DOI Listing
May 2014

Deletion 1q43 encompassing only CHRM3 in a patient with autistic disorder.

Eur J Med Genet 2013 Feb 16;56(2):118-22. Epub 2012 Dec 16.

Department of Pediatrics, 601 Elmwood Ave., University of Rochester Medical Centre, Rochester, NY 14642, USA.

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http://dx.doi.org/10.1016/j.ejmg.2012.11.003DOI Listing
February 2013

GRM7 variants associated with age-related hearing loss based on auditory perception.

Hear Res 2012 Dec 25;294(1-2):125-32. Epub 2012 Oct 25.

Thomas H. Gosnell School of Life Sciences, Rochester Institute of Technology, 153 Lomb Memorial Dr. Rochester, NY 14623, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S037859551200209
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http://dx.doi.org/10.1016/j.heares.2012.08.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705704PMC
December 2012

Process of discovery: a fourth-year translational science course.

Med Educ Online 2011 5;16. Epub 2011 Dec 5.

Department of Orthopaedics and Rehabilitation, University of Rochester Medical Center, Rochester, NY, USA.

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http://dx.doi.org/10.3402/meo.v16i0.8443DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3230242PMC
May 2012

Single-nucleotide polymorphisms in the KCNN3 gene associate with preterm birth.

Reprod Sci 2011 Mar 25;18(3):286-95. Epub 2011 Jan 25.

1Department of Obstetrics and Gynecology, University of Iowa Carver College of Medicine, Iowa City, IA, USA.

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http://dx.doi.org/10.1177/1933719110391277DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053422PMC
March 2011

Young-Simpson syndrome (YSS), a variant of del(1)(p36) syndrome?

Am J Med Genet A 2008 Jun;146A(12):1571-4

Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Golisano Children's Hospital at Strong, Rochester, New York, USA.

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http://dx.doi.org/10.1002/ajmg.a.32096DOI Listing
June 2008

Genetics in medical school curriculum: a look at the University of Rochester School of Medicine and Dentistry.

J Zhejiang Univ Sci B 2008 Jan;9(1):10-5

Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

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http://dx.doi.org/10.1631/jzus.B073004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2170463PMC
January 2008

Transverse craniofacial features and their genetic predisposition in families with nonsyndromic unilateral cleft lip and palate.

Cleft Palate Craniofac J 2004 May;41(3):256-61

Eastman Department of Dentistry, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14620, USA.

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http://dx.doi.org/10.1597/02-134.1DOI Listing
May 2004

Association of nasomaxillary asymmetry in children with unilateral cleft lip and palate and their parents.

Cleft Palate Craniofac J 2003 Sep;40(5):493-7

Eastman Department of Dentistry, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14620, USA.

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http://dx.doi.org/10.1597/1545-1569_2003_040_0493_aonaic_2.0.co_2DOI Listing
September 2003

Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.

Nat Genet 2002 Mar 11;30(3):321-4. Epub 2002 Feb 11.

Human Medical Genetics Program, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.

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http://dx.doi.org/10.1038/ng835DOI Listing
March 2002