Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci.
about
Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer familiesConstitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.Loss of heterozygosity in lobular carcinoma in situ of the breast.Linkage analysis of chromosome 17q markers and breast-ovarian cancer in Icelandic families, and possible relationship to prostatic cancer.THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21.Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21Linkage analysis of 19 French breast cancer families, with five chromosome 17q markers.Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindredsChromosome 17q linkage studies of 18 Utah breast cancer kindreds.Linkage analysis in German breast cancer families with early onset of the disease, using highly polymorphic markers from the chromosome 17q11-q24 regionClosing in on a breast cancer gene on chromosome 17q.Immunogenetics of leishmanial and mycobacterial infections: the Belem Family Study.A search for evidence of somatic mutations in the NF1 gene.A comparison of methods for gene dosage analysis in HMSN type 1.Low level microsatellite instability may be associated with reduced cancer specific survival in sporadic stage C colorectal carcinoma.An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium.Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.Genetic instability in human ovarian cancer cell lines.Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients.Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardationAllelic imbalance in the region of the BRCA1 gene in ductal carcinoma in situ of the breastFunctional evidence for a second tumor suppressor gene on human chromosome 17.Infrequent loss of heterozygosity of APC/MCC and DCC genes in gastric cancer showing DNA microsatellite instability.An unconditional exact test for the Hardy-Weinberg equilibrium law: sample-space ordering using the Bayes factor.Linkage analysis of BRCA1 in Japanese breast cancer families.Frequent genetic instability in small intestinal carcinomas.
P2860
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P2860
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci.
@en
type
label
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci.
@en
prefLabel
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci.
@en
P2093
P1476
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci
@en
P2093
A E Kwitek
D H Ledbetter
F S Collins
M R Wallace
P2860
P577
1990-08-01T00:00:00Z