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A deletion in exon 9 of the LIPH gene is responsible for the rex hair coat phenotype in rabbits (Oryctolagus cuniculus)Fine characterisation of a recombination hotspot at the DPY19L2 locus and resolution of the paradoxical excess of duplications over deletions in the general populationMutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostosesA 5' splice site mutation in fucosidosisArginine 109 to glutamine mutation in a girl with ornithine carbamoyl transferase deficiencyNiemann-Pick C1 disease: correlations between NPC1 mutations, levels of NPC1 protein, and phenotypes emphasize the functional significance of the putative sterol-sensing domain and of the cysteine-rich luminal loop.Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.Exposure to violence during childhood is associated with telomere erosion from 5 to 10 years of age: a longitudinal studyPelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisMalignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscleSequence analysis of Drd2, Drd4, and Dat1 in SHR and WKY rat strains.Factor H and CFHR1 polymorphisms associated with atypical Haemolytic Uraemic Syndrome (aHUS) are differently expressed in Tunisian and in Caucasian populations.The scurs inheritance: new insights from the French Charolais breed.The immune response to the HPA-1a antigen: association with HLA-DRw52a.T cell receptor beta chain polymorphisms are associated with cystic fibrosis.Mapping of the X linked form of hyper IgM syndrome (HIGM1)A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.Molecular mechanisms in Angelman syndrome: a survey of 93 patients.Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland.Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.Carrier estimations in Duchenne muscular dystrophy families in Northern Ireland using RFLP analysisA genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkageBecker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy.Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellitesMutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresisInternalizing disorders and leukocyte telomere erosion: a prospective study of depression, generalized anxiety disorder and post-traumatic stress disorder.A test of the double-strand break repair model for meiotic recombination in Saccharomyces cerevisiae.A genetic linkage map of the male goat genome.Niemann-Pick disease type C: spectrum of HE1 mutations and genotype/phenotype correlations in the NPC2 group.Restricted genetic variation in populations of Achatina (Lissachatina) fulica outside of East Africa and the Indian Ocean Islands points to the Indian Ocean Islands as the earliest known common source.Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on BrainCharacterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene.Perinatal complications and aging indicators by midlife.Is chronic asthma associated with shorter leukocyte telomere length at midlife?BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families.Allele-specific methylation and expression of an imprinted U2af1-rs1 (SP2) gene.Genetic Predisposition to Diabetic Nephropathy: Evidence for a Role of ACE (I/D) Gene Polymorphism in Type 2 Diabetic Population from Kutch RegionMutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman disease.Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).
P2860
Q21135469-FC9AD731-8A48-49EB-8AF8-29D5651D3CC2Q21144892-7A3E220A-603F-4EE6-9318-D89328E735E7Q24316959-FF09DA71-3D12-4EAD-8E10-E47C682CACABQ24514978-3A06312F-10A2-4828-9FEF-294C54339AA3Q24515023-1DA3A1D8-5D33-4E5E-83D2-63CB13806C72Q24533516-792E9D9E-6317-4440-8A01-6AD9F85B1DBAQ24535825-6D1CD1C4-1F31-4501-B9BE-355539DD2E68Q24595920-3B350803-A16C-4412-9B54-9C8ED38AD2E1Q24669755-47BD2277-D6AC-4320-B430-8242E51A502FQ24676753-A8282748-2289-4629-913B-8ADA25108590Q25255814-9339797E-4299-40CA-A38D-05D2CC4E530DQ33398546-A3C2A7C2-FD2B-4114-9F68-71FDBCE97263Q33478033-D06BB82F-6D2D-40CA-9B0B-50A338D5F326Q33500029-B39D6BB8-920C-46F3-8F90-5DCA99836029Q33593095-1E744281-DFF3-45AD-889C-AF0F43B0A4E6Q33595078-EA5E4799-9483-4DA5-92E5-1F4771185D04Q33595272-EB8F1DC3-A1FC-4C53-97BF-8A070EA83551Q33595511-8C38889A-B9CA-4C4B-BA5F-87A82CD05742Q33595952-3632C1B3-E1FB-4F00-996E-2EA2259C04C7Q33596099-ABC68812-13BF-4A44-881C-3F9AC64ED3F4Q33596253-1A70BBCF-F060-4DAD-879A-4D2DC6BCC3FEQ33597177-94423536-2604-470F-A9C2-4E08AD770A79Q33597748-33CF174C-8F46-40F2-BB91-1311601FF94FQ33597923-29868563-CA96-4071-BE8A-1E454C8F4BA6Q33675544-36150FAB-E609-45FC-8EAE-8C80C7EDB59AQ33862158-713B5E16-D127-47B1-8341-FCB2D18F6582Q33901278-CB8064DF-51DB-40DA-8BE1-BBF5DD873F4EQ33968364-CFBFB688-8FF7-4F93-B910-BC835B23699AQ33968370-836DDA46-5CA5-4A6E-9B77-08B70788B436Q34112998-8D98D772-341D-4FCE-9E61-DA13C6D32AF4Q34155586-DBDB4C90-B1EF-451F-A492-E14A7C19D23BQ34389940-AA9F8D48-0E96-4188-9BDA-29F955DEAB78Q34390757-EB6AD9B6-A27F-476A-BDC3-D522A716A25AQ34411264-5BB2EC93-B9C0-4F4E-97D6-02A6088BF583Q34425969-D984C08B-9F08-41E6-9A2B-F22A2C8AE747Q34480647-8640ACAB-C0EB-47B6-9430-421AFD746C10Q34733341-F7E1750A-706D-493A-A842-2231D60F8306Q35028043-E3367C52-B701-4EC7-BEE7-25A8AFE5032AQ35129861-7D80811A-DBF3-4F90-BD96-8169728F0300Q35194574-81A6163C-5AA4-4A2C-BE02-4905FEAEB3CC
P2860
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
A rapid method for the purification of DNA from blood.
@en
type
label
A rapid method for the purification of DNA from blood.
@en
prefLabel
A rapid method for the purification of DNA from blood.
@en
P356
P1476
A rapid method for the purification of DNA from blood.
@en
P2093
Jeanpierre M
P356
10.1093/NAR/15.22.9611
P577
1987-11-01T00:00:00Z