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Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.
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Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disorders.
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Rare germline disorders implicate long non-coding RNAs disrupted by chromosomal structural rearrangements.
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Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency.
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Reproductive Risk Estimation Calculator for Balanced Translocation Carriers.
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Array-comparative Genomic Hybridization Results in Clinically Affected Cases with Apparently Balanced Chromosomal Rearrangements.
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Disruption of neurexin 1 associated with autism spectrum disorder.
Am J Hum Genet. 2008 Jan;82(1):199-207. doi: 10.1016/j.ajhg.2007.09.011.
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Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
Am J Med Genet A. 2007 Nov 15;143A(22):2668-74. doi: 10.1002/ajmg.a.32034.
3
Rearrangements involving 12q in myeloproliferative disorders: possible role of HMGA2 and SOCS2 genes.
Cancer Genet Cytogenet. 2007 Jul 1;176(1):80-8. doi: 10.1016/j.cancergencyto.2007.03.009.
5
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
PLoS Genet. 2007 May 25;3(5):e80. doi: 10.1371/journal.pgen.0030080.
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Rapid high-resolution karyotyping with precise identification of chromosome breakpoints.
Genes Chromosomes Cancer. 2007 Jul;46(7):675-83. doi: 10.1002/gcc.20452.
7
Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice.
Am J Hum Genet. 2007 Apr;80(4):792-9. doi: 10.1086/513019. Epub 2007 Feb 12.
8
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.
Am J Hum Genet. 2007 Apr;80(4):616-32. doi: 10.1086/512735. Epub 2007 Feb 14.
9
Disruption of a synaptotagmin (SYT14) associated with neurodevelopmental abnormalities.
Am J Med Genet A. 2007 Mar 15;143A(6):558-63. doi: 10.1002/ajmg.a.31618.
10
Candidate loci for Zimmermann-Laband syndrome at 3p14.3.
Am J Med Genet A. 2007 Jan 15;143A(2):107-11. doi: 10.1002/ajmg.a.31544.

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