Nicole Bain

Nicole Bain

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Nicole Bain

Nicole Bain

Publications by authors named "Nicole Bain"

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12Publications

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Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1R.

Eur J Med Genet 2016 Apr 12;59(4):257-62. Epub 2015 Dec 12.

Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2015.12.002DOI Listing
April 2016

Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions.

Eur J Med Genet 2015 Nov 23;58(11):629-33. Epub 2015 Oct 23.

Hunter Genetics, Newcastle, New South Wales, Australia; The University of Newcastle, School of Medicine and Public Health, Newcastle, New South Wales, Australia.

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http://dx.doi.org/10.1016/j.ejmg.2015.10.006DOI Listing
November 2015

A familial 7q36.3 duplication associated with agenesis of the corpus callosum.

Am J Med Genet A 2015 Sep 5;167A(9):2201-8. Epub 2015 May 5.

The University of Newcastle, School of Medicine and Public Health, Newcastle, New South Wales, Australia.

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http://dx.doi.org/10.1002/ajmg.a.37143DOI Listing
September 2015

16p13.11 microdeletion in a patient with hemiconvulsion-hemiplegia-epilepsy syndrome: a case report.

J Child Neurol 2015 Jan 21;30(1):83-6. Epub 2014 Jan 21.

The University of Newcastle, School of Medicine and Public Health, Newcastle, New South Wales, Australia Hunter Genetics, Newcastle, New South Wales, Australia.

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http://dx.doi.org/10.1177/0883073813516382DOI Listing
January 2015

Outfoxed by RBFOX1-a caution about ascertainment bias.

Am J Med Genet A 2014 Jun 24;164A(6):1411-8. Epub 2014 Mar 24.

Hunter Genetics, Newcastle, New South Wales, Australia; The University of Newcastle, School of Medicine and Public Health, Newcastle, New South Wales, Australia.

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http://dx.doi.org/10.1002/ajmg.a.36458DOI Listing
June 2014

An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.

Eur J Med Genet 2014 Feb 22;57(2-3):65-70. Epub 2014 Jan 22.

Hunter Genetics, Newcastle, PO Box 84, Waratah, NSW 2298, Australia; University of Newcastle, Newcastle - School of Medicine and Public Health, Faculty of Health, Level 1, Bowman Building, Callaghan, NSW 2308, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2013.12.011DOI Listing
February 2014

Genomic profiling of plasma cell disorders in a clinical setting: integration of microarray and FISH, after CD138 selection of bone marrow.

J Clin Pathol 2014 Jan 22;67(1):66-9. Epub 2013 Aug 22.

Department of Haematology, Calvary Mater Hospital, , Newcastle, New South Wales, Australia.

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http://dx.doi.org/10.1136/jclinpath-2013-201691DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888588PMC
January 2014

FOXP1 mutations cause intellectual disability and a recognizable phenotype.

Am J Med Genet A 2013 Dec 24;161A(12):3166-75. Epub 2013 Sep 24.

Hunter Genetics, Newcastle, NSW, Australia; John Hunter Children's Hospital, Newcastle, NSW, Australia.

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http://dx.doi.org/10.1002/ajmg.a.36174DOI Listing
December 2013

Clinical features associated with a 15.41 Mb deletion of chromosome 13q encompassing the MIR17HG locus.

Clin Dysmorphol 2013 Apr;22(2):68-70

University of Newcastle, Callaghan, New South Wales, Australia.

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http://dx.doi.org/10.1097/MCD.0b013e32835f56b3DOI Listing
April 2013

Weight and muscularity concerns as longitudinal predictors of body image among early adolescent boys: a test of the dual pathways model.

Body Image 2008 Jun 23;5(2):195-204. Epub 2008 May 23.

University of Washington, Seattle, WA 98195-3600, USA.

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http://dx.doi.org/10.1016/j.bodyim.2007.12.001DOI Listing
June 2008