about
Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epitheliumThe human enamel protein gene amelogenin is expressed from both the X and the Y chromosomesNeural-specific expression, genomic structure, and chromosomal localization of the gene encoding the zinc-finger transcription factor NGFI-CTwo human glutamate decarboxylases, 65-kDa GAD and 67-kDa GAD, are each encoded by a single geneCloning, heterologous expression, and chromosomal localization of human inositol polyphosphate 1-phosphataseAnalysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinismCloning and in vivo expression of the human GART gene using yeast artificial chromosomesA compositional map of human chromosome band Xq28Molecular genetics of steroid 5 alpha-reductase 2 deficiencyA GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptorsUniparental disomy as a mechanism for human genetic diseaseCloning of a candidate gene for ataxia-telangiectasia group DHuman molecular cytogenetics: From cells to nucleotidesReciprocal translocation 14q;21q in a patient with the Brachmann-de Lange syndromeSilver staining of selected mitoses by physical development.Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromere.Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome.X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.Partial trisomy 7p associated with familial 7p;22q translocationX-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome.A case of two inversion (10) recombinants in a family.Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivativesMolecular and cytogenetic studies of the Prader-Willi syndrome.A case of partial 5q trisomy associated with partial 7q monosomy.High resolution of a small pericentric inversion of chromosome 11.Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings.The X linked recessive form of XY gonadal dysgenesis with a high incidence of gonadal germ cell tumours: clinical and genetic studiesThe fragile X: a scanning electron microscope studyLocation of the retinoblastoma susceptibility gene(s) and the human esterase D locus.Partial trisomy 16p due to maternal balanced translocation.Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous aborters.De novo paracentric inversion in an X chromosome.Segregation of a t(3;20) translocation through three generations resulting in unbalanced karyotypes in six persons.A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasiaDetection of centromeric regions of chromosomes by immunofluorescence: procedure and application.Chromosome subband 17p11.2 deletion: a minute deletion syndrome.Schizophrenia susceptibility gene locus at Xp22.3.Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern.Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.
P2860
Q22009003-57A81B76-BA9D-4697-8603-A9D5CC3E441CQ24299358-D57AA27E-F2CD-4BD2-9A84-B62253326A37Q24300587-7C4586A7-059C-49E6-B2F3-ACE6015444C4Q24307858-CBAE8D47-C84A-4A43-B5C4-ABC3B53BDC97Q24316002-AD099F73-F212-407D-A83C-BDF121144737Q24514987-7C815E95-4180-41A9-A979-B69775ED42BEQ24561450-292E268A-AA4E-41F7-AE2E-72FAAA9E9D79Q24567545-85BDD63E-0AD4-4B25-80D3-B6B495BBAFD5Q24619385-AFA57E7E-6C96-4153-8A87-28ABAFD472B0Q24676257-8B2644D9-72CD-45F9-ABC5-8BCD0E433DE4Q24679370-E2A5E153-0242-4FDC-AC2B-1837D4B42A88Q24679645-ED324AE5-EEB5-4EA8-8E37-DD80B4EFDE63Q27024633-4402F349-0871-4977-8FFB-980F64E2AB82Q30443066-50881C4E-A3FA-477B-9021-14A1F12350DCQ31443723-32C5DB41-987D-4D1D-96AE-D403AD1927E0Q31912726-A8F5BB07-C13A-4B24-B33E-5C247604C3DAQ33325218-537A6592-0E31-44D9-9D81-A544888D31B0Q33584573-8BF37736-390E-43CC-A535-F26CFADA8D1BQ33587681-FA77AC37-BAAB-411A-81C0-2F30E62FC366Q33588425-C6DBFBA3-D528-4A40-8B40-D24A94633236Q33593100-63B5E1CF-E12E-4B19-A92F-EDC40AD38860Q33593123-A8FA60B0-28FC-43C4-8BBD-E7C672D9A4F9Q33593354-5D5C6DD2-B4E8-4B16-BFFF-742AF087AB47Q33597595-3915A837-CA6E-4439-A229-36621113A19EQ33644632-71B0AE43-E359-4C42-92B9-211E5EED1674Q33667674-D9A8381D-C1BC-4D65-855D-C9797C4BD88EQ33668144-229FB460-BD6A-4CDD-8F0F-52A9019540FBQ33670718-F891F771-FD93-4F3D-8C61-24010037E884Q33670739-1D833A67-D03F-4DFA-8960-255F55521245Q33671171-156F6CDB-84AD-4854-8AB0-A57D811EE6ACQ33671501-853E70B0-1B85-4DE3-9F54-376403742640Q33671793-3CD47DBF-E9B9-4FE1-8515-0146F321D3EBQ33671931-548596B0-ED34-4F7F-BC14-5EE96186665DQ33673742-371FAE4A-B52B-4899-90B3-94DE545AAD67Q33675302-1F99F563-4E02-4122-8061-416AD7B2EA70Q33675645-A9A9329B-2AF3-4459-B83E-E1200C73C158Q33682019-8D4176A2-0C6F-4424-8783-FE9759CC22B1Q33713536-783494CC-C2B1-420C-8889-A87F24CB9289Q33792567-3BFEF003-70D0-4D12-AAD1-4C0ECE3DBC00Q33864953-FDC3B84A-0A95-4E8E-9420-3E4E2644C833
P2860
description
1976 nî lūn-bûn
@nan
1976 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1976 թվականի մարտին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
High resolution of human chromosomes.
@ast
High resolution of human chromosomes.
@en
High resolution of human chromosomes.
@nl
type
label
High resolution of human chromosomes.
@ast
High resolution of human chromosomes.
@en
High resolution of human chromosomes.
@nl
prefLabel
High resolution of human chromosomes.
@ast
High resolution of human chromosomes.
@en
High resolution of human chromosomes.
@nl
P356
P1433
P1476
High resolution of human chromosomes.
@en
P2093
P304
P356
10.1126/SCIENCE.1257746
P407
P577
1976-03-01T00:00:00Z