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p99-6

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編號(hào):B206821

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產(chǎn)品名稱	p99-6
商品貨號(hào)	B206821
Designations	p99-6
Species	Homo sapiens, human
Applications	Multipoint linkage analysis shows complete linkage (LOD score = 7.07).
Vector	Construct size (kb): 4.050000190734863
Insert	DNA: genomic Insert lengths(kb): 1.399999976158142 Tissue: lymphoblast (49,XXXXY) cell line Gene product: DNA Segment, single copy [DXS41] Alleles: A1, A2
Insert Size (kb)	1.400
Biosafety Level	1 Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Shipping Information	Distributed: DNA (dried). Rehydrate with TE. (amount: 2 ug)
Comments	This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 3.44). Multipoint linkage analysis shows complete linkage (LOD score = 7.07).
References	Aldridge J, et al. A strategy to reveal high-frequency RFLPs along the human X chromosome. Am. J. Hum. Genet. 36: 546-564, 1984. PubMed: 6328976 Stambolian D, et al. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis. Am. J. Hum. Genet. 47: 13-19, 1990. PubMed: 1971992 Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 Thakker RV, et al. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics 8: 189-193, 1990. PubMed: 1979046 Francke U, et al. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions. Am. J. Hum. Genet. 40: 212-227, 1987. PubMed: 2883886

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