Digital Library
Close Browse articles from a journal
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
                                       All articles of the corresponding issues
 
                             28 results found
no title author magazine year volume issue page(s) type
1 A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture Khandjian, Edouard W.
1995
4 5 p. 783-789
article
2 A homozygous nonsense mutation in the α3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa Kivirikko, Sirpa
1995
4 5 p. 959-962
article
3 A human homolog of the S.cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region Lamour, Valé
1995
4 5 p. 791-799
article
4 A novel dystrophin isoform is required for normal retinal electrophysiology D'Souza, Vinita N.
1995
4 5 p. 837-842
article
5 A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q Vincent, P.
1995
4 5 p. 945-949
article
6 Author index 1995
4 5 p. 973-973
article
7 Characterization of FMR1 proteins isolated from different tissues Verhell, Coleta
1995
4 5 p. 895-901
article
8 Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) Lunt, Peter W.
1995
4 5 p. 951-958
article
9 CORRIGENDUM Borish, L.
1995
4 5 p. 974-974
article
10 CORRIGENDUM Kobayashi, K.
1995
4 5 p. 974-974
article
11 Definition of the blepharophimosis, ptosis, epicanthus inversus syndrome critical region at chromosome 3q23 based on the analysis of chromosomal anomalies Lawson, Claire T.
1995
4 5 p. 963-967
article
12 ERRATUM Telenius, H.
1995
4 5 p. 974-974
article
13 High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes Florijn, Ralpha J.
1995
4 5 p. 831-836
article
14 Human cell mutants with very low mitochondrial DNA copy number (ρd) Vaillant, François
1995
4 5 p. 903-914
article
15 Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region Bergen, Arthur A.B.
1995
4 5 p. 931-935
article
16 Mitochondrial DNA diversity in the Kuna Amerinds of Panamá Batista, Oriana
1995
4 5 p. 921-929
article
17 Molecular analysis of type II 3β-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3β-hydroxysteroid dehydrogenase deficiency Tajima, Toshihiro
1995
4 5 p. 969-971
article
18 Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease Maruyama, Hirofumi
1995
4 5 p. 807-812
article
19 Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease Angrist, Misha
1995
4 5 p. 821-830
article
20 Neurofibromatosis 1 (NF1) mRNAs expressed in the central nervous system are differentially spliced in the 5′ part of the gene Danglot, Glséle
1995
4 5 p. 915-920
article
21 No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease Liddell, Malcolm B.
1995
4 5 p. 853-858
article
22 Nucleotide sequence analysis of the apolipoprotein B 3′ VNTR Ellsworth, Darrell L.
1995
4 5 p. 937-944
article
23 Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews Glaser, Benjamin
1995
4 5 p. 879-886
article
24 Sex-specific meiotic recombination in the Prader—Willi/Angelman syndrome imprinted region Robinson, Wendy P.
1995
4 5 p. 801-806
article
25 Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus Jansen, Gert
1995
4 5 p. 843-852
article
26 The distribution of linkage disequilibrium over anonymous genome regions Peterson, Amy C.
1995
4 5 p. 887-894
article
27 The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability Klink, Albrecht
1995
4 5 p. 869-878
article
28 The human Y chromosome homologue of XG: transcription of a naturally truncated gene Weller, Polly A.
1995
4 5 p. 859-868
article
                             28 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands