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virtual library in human genetics and molecular biology

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA
C Huxley, E Passage, A Manson, G Putzu, D Figarella-Branger, J F Pellissier and M Fontes
P. 563

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development
M A Crackower, S W Scherer, J M Rommens, C-C Hui, P Poorkaj, S Soder, J M Cobben, L Hudgins, J P Evans and L-C Tsui
P. 571

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35
J C T van Deutekom, R J L F Lemmers, P K Grewal, M van Geel, S Romberg, H G Dauwerse, T J Wright, G W Padberg, M H Hofker, J E Hewitt and R R Frants
P. 581

Gene transfer into the mouse retina mediate by an adeno- associated viral vector
R R Ali, M B Reichel, A J Thrasher, R J Levinsky, C Kinnon, N Kanuga, D M Hunt and S S Bhattacharya
P. 591

Isolation of genes amplified in human cancers by microdissection mediated by cDNA capture
E Gracia, U Fischer, A ElKahloun, J M Trent, E Meese and P S Meltzer
P. 595

Mutations in the Ca2+ sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism
J Baron, K K Winer, J A Yanovski, A W Cunningham, L Laue, D Zimmerman and G B Cutler, Jr
P. 601

cDNA cloning of a human homologue of the C. elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat
R L Margolis, O C Stine, M G McInnis, N G Ranen, D C Rubinsztein, J Leggo, L V Jones Brando, A S Kidwai, S J Loev, T S Breschel, C Callahan, S G Simpson, J R DePaulo, F J McMahon, S Jain, E S Paykel, C Walsh, L E DeLisi, T J Crow, E F Torrey, R G Ashworth, J P Macke, J Nathans and C A Ross
P. 607

Isolation of a new clathrin heavy chain gene with muscle- specific expression from the region commonly deleted in velo-cardio-facial syndrome
H Sirotkin, B Morrow, R DasGupta, R Goldberg, S R Patanjali, G Shi, L Cannizzaro, R Shprintzen, S M Weissman and R Kucherlapati
P. 617

Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11
D Kedra, M Peyrard, I Fransson, J E Collins, I Dunham, B A Roe and J P Dumanski
P. 625

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes
S Demczuk, G Thomas and A Aurias
P. 633

Expression of the von Hippel-Landau disease tumour suppression gene during human embryogenesis
F M Richards, P N Schofield, S Fleming and E R Maher
P. 639

Crigler-Najjer syndrome type II is inherited both as a dominant and as a recessive trait
O Koiwai, S Aono, Y Adachi, T Kamisako, Y Yasui, M Nishizawa and H Sato
P. 645

X-linked liver glycogenosis type II (XLG II) is caused by mutations in PHKA2, the gene encoding the liver alpha subunit of phosphorylase kinase
J Hendrickx, E Dams, P Coucke, P Lee, J Fernandes and P J Willems
P. 649

Mutation hotspots in the PHKA2 gene in X-linked liver glycogenesis due to phosphorylase kinase deficiency with atypical activity in blood cells (XLG2)
B Burwinkel, Y S Shin, H D Bakker, J Deutsch, M J Lozano, I Maire and M W Kilimann
P. 653

Long-range sequence analysis in Xq28: 13 known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci
E Y Chen, M Zollo, R Mazzarella, A Ciccodicola, C-n Chen, L Zuo, C Heiner, F Burough, M Repetto, D Schlessinger and M D'Urso
P.659

Genetic mapping of the human homologue (T) of mouse T (Brachyury) and a search for allele association between human T and spina bifida
K Morrison, C Papapetrou, J Attwood, F Hol, S A Lynch, A Sampath, B Hamel, J Burn, J Sowden, D Stott, E Mariman and Y H Edwards
P. 669

A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding region
A M Theodosiou, N R Rodrigues, M A Nesbit, H J Ambrose, H Paterson, E. McLellan-Arnold, Y Boyd, M A Leversha, N Owen, D J Blake, A Ashworth and K E Davies
P.675

Heterogeneity in telomere length of human chromosomes
P M Lansdorp, N P Verwoerd, F M van de Rijke, V Dragowska, M-T Little, R W Dirks, A K Raap and H J Tanke
P. 685

Confirmation of three susceptibility genes to insulin- dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8
D-F Luo, R Buzzetti, J I Rotter, N K Maclaren, L J Raffel, L Nistico, C Giovannini, P Pozzilli, G Thomson and J-X She
P.693

Linkage of polymorphic congenital cataract to the gamma- crystallin gene locus on human chromosome 2q33-35
E I Rogaev, E A Rogaeva, G I Korovaitseva, L A Farrer, A N Petrin, S A Keryanov, S Turaeva, I Chumakov, P St. George-Hyslop and E K Ginter
P. 699

Localisation of a gene for central areolar choroidal dystrophy to chromosome 17p
A J Lotery, K T Ennis, G Silvestri, S Nicholl, D McGibbon, A D Collins and A E Hughes
P. 705

Human Molecular Genetics is a monthly journal of original peer-reviewed research, published by Oxford University Press.
In addition to the regular monthly issues, a special review issue, reviewing important developments in the field, is published each year.

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