Kamnasaran D - Search Results

1

Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes.

Kamnasaran D, O'Brien PC, Schuffenhauer S, Quarrell O, Lupski JR, Grammatico P, Ferguson-Smith MA, Cox DW. Kamnasaran D, et al. Am J Med Genet. 2001 Aug 1;102(2):173-82. doi: 10.1002/ajmg.1418. Am J Med Genet. 2001. PMID: 11477612

2

Rearrangement in the PITX2 and MIPOL1 genes in a patient with a t(4;14) chromosome.

Kamnasaran D, O'Brien PC, Zackai EH, Muenke M, Ferguson-Smith MA, Cox DW. Kamnasaran D, et al. Eur J Hum Genet. 2003 Apr;11(4):315-24. doi: 10.1038/sj.ejhg.5200963. Eur J Hum Genet. 2003. PMID: 12700605

3

Comparative mapping of human Chromosome 14q11.2-q13 genes with mouse homologous gene regions.

Kamnasaran D, O'Brien PC, Ferguson-Smith MA, Cox DW. Kamnasaran D, et al. Mamm Genome. 2000 Nov;11(11):993-9. doi: 10.1007/s003350010183. Mamm Genome. 2000. PMID: 11063256

4

Current status of human chromosome 14.

Kamnasaran D, Cox DW. Kamnasaran D, et al. J Med Genet. 2002 Feb;39(2):81-90. doi: 10.1136/jmg.39.2.81. J Med Genet. 2002. PMID: 11836355 Free PMC article. Review.

5

Disruption of the neuronal PAS3 gene in a family affected with schizophrenia.

Kamnasaran D, Muir WJ, Ferguson-Smith MA, Cox DW. Kamnasaran D, et al. J Med Genet. 2003 May;40(5):325-32. doi: 10.1136/jmg.40.5.325. J Med Genet. 2003. PMID: 12746393 Free PMC article.

6

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes.

Kamnasaran D, Chen CP, Devriendt K, Mehta L, Cox DW. Kamnasaran D, et al. Genomics. 2005 May;85(5):608-21. doi: 10.1016/j.ygeno.2005.01.010. Genomics. 2005. PMID: 15820313

7

Features within the holoprosencephaly spectrum in sibs with a Robertsonian (14q;22q) translocation chromosome.

Kamnasaran D, Gerritsen JA, McLeod DR, Cox DW. Kamnasaran D, et al. Clin Genet. 2001 Sep;60(3):237-9. doi: 10.1034/j.1399-0004.2001.600311.x. Clin Genet. 2001. PMID: 11595027 No abstract available.

8

Epigenetic inheritance associated with human chromosome 14.

Kamnasaran D. Kamnasaran D. Clin Invest Med. 2001 Jun;24(3):138-46. Clin Invest Med. 2001. PMID: 11437065 Review.

9

Current perspectives on the etiology of agnathia-otocephaly.

Gekas J, Li B, Kamnasaran D. Gekas J, et al. Among authors: kamnasaran d. Eur J Med Genet. 2010 Nov-Dec;53(6):358-66. doi: 10.1016/j.ejmg.2010.09.002. Epub 2010 Sep 16. Eur J Med Genet. 2010. PMID: 20849990 Review.

10

Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.

Sergi C, Gekas J, Kamnasaran D. Sergi C, et al. Among authors: kamnasaran d. Fetal Pediatr Pathol. 2012 Oct;31(5):315-8. doi: 10.3109/15513815.2012.659390. Epub 2012 Mar 20. Fetal Pediatr Pathol. 2012. PMID: 22432933

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