about
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.Genetic analysis of haemophilia A in BulgariaLithuanian haemophilia A and B registry comprising phenotypic and genotypic data.Refining the genetic location of the gene for X linked hydrocephalus within Xq28.Fine mapping of the dyskeratosis congenita locus in Xq28.Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study.Gonadal mosaicism for incontinentia pigmenti in a healthy male.X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studiesThe gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28Rapid polymerase chain reaction analysis of St14 (DXS52) VNTR: carrier detection of hemophilia A.Unrelated donor cord blood transplantation in adults with chronic myelogenous leukemia: results in nine patients from a single institution.Polymorphisms associated with the FVIII and FIX genes in the Turkish population.Importance of mixed chimerism to predict relapse in persistently BCR/ABL positive long survivors after allogeneic bone marrow transplantation for chronic myeloid leukemia.Prevalence of chimerism after non-myeloablative hematopoietic stem cell transplantation.CD45 isoform phenotypes of human T cells: CD4(+)CD45RA(-)RO(+) memory T cells re-acquire CD45RA without losing CD45RO.Reduction of end-stage malignant glioma by injection with autologous cytotoxic T lymphocytes.
P2860
Q24540280-1EC7ADF4-B6F0-4B03-BC68-A2536068676FQ24805057-EB0A1E4E-528C-40BE-B416-B763BFC05338Q30647406-F11C6AEC-BEB6-40AF-8FF9-8D7CB16E7A0FQ33595095-3BA17D5B-C2E3-40ED-B4AE-09D9A2503816Q33678095-B0936D7E-4B83-441A-839A-677C6B41D71DQ33681535-06F46669-0AA7-435B-860B-EE9307FA4656Q33682795-C15DF8C4-2565-44E7-B2CB-1455F8A4BBB2Q35196067-081261B2-CEEC-4C70-9CEB-2EEDC3579F6BQ35644329-36011376-FDDF-4A52-9550-A9B5F5553FEBQ35881835-C88D0F6D-071B-4443-8149-E0D7AAC94D40Q35882720-F93E7821-E0EE-411E-A538-EF606B40D35CQ40884820-3B8847DB-FE0D-48D8-BF49-37EC1DAD2C2BQ43613017-67944815-23B2-4298-8C92-2AB1B007EBCDQ45886843-248390F9-5D7F-4EF8-86F4-B760B3E87BD8Q48011084-0FAE3AB1-E36A-4489-A6A8-608D2B2B5999Q51582474-2D437D15-242D-4777-986C-591796316C61Q52030364-EAEC10A5-3FDC-446D-B057-67BF34307168Q54956863-53D8CF06-58D8-4ED3-9AEA-5F356C9495CE
P2860
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh
1991年學術文章
@zh-hant
name
Rapid PCR analysis of the St14 (DXS52) VNTR.
@en
type
label
Rapid PCR analysis of the St14 (DXS52) VNTR.
@en
prefLabel
Rapid PCR analysis of the St14 (DXS52) VNTR.
@en
P2093
P356
P1476
Rapid PCR analysis of the St14 (DXS52) VNTR.
@en
P2093
P2860
P356
10.1093/NAR/19.8.1944
P577
1991-04-01T00:00:00Z