Publications by authors named "Sulekha Rajagopalan"

14Publications

Infant with hypopigmented streaks.

J Paediatr Child Health 2019 Sep;55(9):1145-1146

The Skin Hospital, Sydney, New South Wales, Australia.

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http://dx.doi.org/10.1111/jpc.1_14548DOI Listing
September 2019

User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia.

J Genet Couns 2019 04 14;28(2):240-250. Epub 2018 Dec 14.

Centre for Clinical Genetics, Sydney Children's Hospital, High St, Randwick, Sydney, NSW, 2031, Australia.

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http://doi.wiley.com/10.1007/s10897-018-0298-5
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http://dx.doi.org/10.1007/s10897-018-0298-5DOI Listing
April 2019

Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.

J Am Coll Cardiol 2018 07;72(4):419-429

Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.jacc.2018.04.078DOI Listing
July 2018

Update on the Diagnosis and Management of Brugada Syndrome.

Heart Lung Circ 2015 Dec 20;24(12):1141-8. Epub 2015 Aug 20.

Department of Clinical Genetics, Liverpool Hospital, Liverpool, NSW, Australia.

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http://dx.doi.org/10.1016/j.hlc.2015.07.020DOI Listing
December 2015

X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations.

Am J Med Genet A 2011 Oct 9;155A(10):2370-80. Epub 2011 Sep 9.

Molecular Genetics Laboratory, GSTS Pathology, Guy's Hospital, London, UK.

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http://dx.doi.org/10.1002/ajmg.a.33913DOI Listing
October 2011