ELIZABETH ROEDER to In Situ Hybridization, Fluorescence
This is a "connection" page, showing publications ELIZABETH ROEDER has written about In Situ Hybridization, Fluorescence.
Connection Strength
0.074
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Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences. J Med Genet. 2023 06; 60(6):547-556.
Score: 0.035
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Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes. Genet Med. 2008 Apr; 10(4):267-77.
Score: 0.013
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Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation. Am J Med Genet A. 2007 Jun 15; 143A(12):1358-65.
Score: 0.012
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Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child. Am J Med Genet. 2000 Dec 18; 95(5):444-9.
Score: 0.008
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Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases. Am J Med Genet. 1998 Dec 28; 80(5):473-80.
Score: 0.007