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  Human Molecular Genetics: April 1997 (Volume 6, No 4)  
  April 01, 1997

virtual library in human genetics and molecular biology

Executive Editors:-
K E Davies, Oxford, UK
Huntington F Willard, Cleveland, OH, USA

Oxford University Press
  Date of publishing: April, 1997  
  ISSN 0261 - 4189SSN 1964-6906


L A Clarke, C S Russell, S Pownall, C L Warrington, A Borowski, J E Dimmick, J Toone and F R Jirik
Murine mucopolysaccharidosis type I: targeted disruption of the murine alpha-L-iduronidase gene P. 503


E N Burright, J D Davidson, L A Duvick, B Koshy, H Y Zoghbi and H T Orr
Identification of a self-association region within the SCA1 gene product, ataxin-1 P. 513

R A Montgomery and H C Dietz
Inhibition of fibrillin-1 expression using U1 snRNA as a vehicle for the presentation of antisense targeting sequence P. 519

A E O Trezise, R Ratcliff, T E Hawkins, M J Evans, T C Freeman, P R Romano, C F Higgins and W H Colledge
Co-ordinate regulation of the cystic fibrosis and multidrug resistance genes in cystic fibrosis knockout mice P. 527

P S N Rowe, C L Oudet, F Francis, C Sinding, S Pannetier, M J Econs, T M Strom, T Meitinger, M Garabedian, A David, M-A Macher, E Questiaux, E Popowska, E Pronicka, A P Read, A Mokrzycki, F H Glorieux, M K Drezner, A Hanauer, H Lehrach, J N Goulding and J L H O'Riordan
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets P. 539

M F Moffatt and W O C M Cookson
Tumour Necrosis Factor haplotypes and asthma P. 551

M E Ross, K M Allen, A K Srivastava, T Featherstone, J G Gleeson, B Hirsch, B N Harding, E Andermann, R Abdullah, M Berg, D Czapansky-Bielman, D J Flanders, R Guerrini, J Motte, A P Mira, I Scheffer, S Berkovic, F Scaravilli, R A King, D H Ledbetter, D Schlessinger, W B Dobyns and C A Walsh
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain P. 555

A Nystuen, H Costeff, O N Elpeleg, N Apter, B Bonne-Tamir, H Mohrenweiser, N Haider, E M Stone and V C Sheffield
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene P. 563

J Nakae, T Tajima, T Sugawara, F Arakane, K Hanaki, T Hotsubo, N Igarashi, Y Igarashi, T Ishii, N Koda, T Kondo, H Kohno, Y Nakagawa, K Tachibana, Y Takeshima, K Tsubouchi, J F Strauss III and K Fujieda
Analysis of the steroidogenic acute regulatory protein (StAR) gene in Japanese patients with congenital lipoid adrenal hyperplasia P. 571

T Arinami, M Gao, H Hamaguchi and M Toru
A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia P. 577

M Vaxillaire, M Rouard, K Yamagata, N Oda, P J Kaisaki, V V Boriraj, J-C Chevre, V Boccio, R D Cox, G M Lathrop, P Dussoix, J Philippe, J Timsit, G Charpentier, G Velho, G I Bell and P Froguel
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3) P. 583

W Hoppner and M M Ritter
A duplication of 12 bp in the critical cysteine rich domain of the RET proto-oncogene results in a distinct phenotype of multiple endocrine neoplasia type 2A P. 587

J D Sharp, R B Wheeler, B D Lake, M Savukoski, I E Jarvela, L Peltonen, R M Gardiner and R E Williams
Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23 P. 591

R E Kelsell, K Evans, C Y Gregory, A T Moore, A C Bird and D M Hunt
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p P. 597

V Nigro, Y Okazaki, A Belsito, G Piluso, Y Matsuda, L Politano, G Nigro, C Ventura, C Abbondanza, A M Molinari, D Acompara, M Nishimura, Y Hayashizaki and G A Puca
Identification of the Syrian hamster cardiomyopathy gene P. 601

M-T Bihoreau, I Ceccherini, J Browne, B Kranzlin, G Romeo, G M Lathrop, M R James and N Gretz
Location of the first genetic locus, PKDr1, controlling autosomal dominant polycystic kidney disease in Han:SPRD cy/+ rat P. 609

V Tiranti, A Savoia, F Forti, M-F D'Apolito, M Centra, M Rocchi and M Zeviani
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database P. 615

K Lagerstedt, S L Karsten, B-M Carlberg, W J Kleijer, T Tonnesen, U Pettersson and M-L Bondeson
Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome P. 627

K Christodoulou, M Tsingis, F Deymeer, P Serdaroglu, C Ozdemir, A Al-Shehab, C Bairactaris, I Mavromatis, I Mylonas, A Evoli, K Kyriallis and L T Middleton
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type 1a) gene to chromosome 17p with evidence of genetic homogeneity P. 635

I Stoilov, A N Akarsu and M Sarfarazi
Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on 2p21 P. 641

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.

The papers listed above will appear in the April 1997 issue, which is shortly to be printed. Copies are scheduled for despatch to subscribers on 20 March 1997.

Copyright in the table of contents listed above is held by Oxford University Press, but you are welcome to circulate them further, provided that Oxford University Press is credited as publisher and copyright holder.

For further information please contact: Journals Subscriptions Department
Oxford University Press
Great Clarendon Street
Oxford OX2 6DP
United Kingdom
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