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K. Prabhakara

Royal Children's Hospital

7

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176

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Extending the scope of diagnostic chromosome analysis: Detection of single gene defects using high-resolution SNP microarrays†

2011 Human Mutation
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Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping

2011 Journal of Medical Genetics
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ASSOCIATION OF PARENTAL HYPERHOMOCYSTEINEMIA AND C677T METHYLENE TETRAHYDROFOLATE REDUCTASE (MTHFR) POLYMORPHISM WITH RECURRENT PREGNANCY LOSS

2009 Clinical Biochemistry
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Prenatal detection of deletion–duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion

2008 Prenatal Diagnosis
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Premature centromere division versus C-anaphases in cultures: Need for consensus and guidelines

2004 American Journal of Medical Genetics Part A
- K. Prabhakara
- A. Radha Ramadevi
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A partial 15q22 trisomy arising due to segregation of maternal 10;15 reciprocal translocation

2002
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De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.

2002 American Journal of Medical Genetics
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Citations (7)