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virtual library in human genetics and molecular biology

ARTICLE

M H Jones, R A Furlong, H Burkin, I J Chalmers, G M Brown, O Khwaja and N A Affara
The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2 P. 1695

REPORTS

Y Yang, S E Haecker, Q Su and J M Wilson
Immunology of gene therapy with adenoviral vectors in mouse skeletal muscle P. 1703

M-C Simmler, D B Cunningham, P Clerc, T Vermat, B Caudron, C Cruaud, A Pawlak, C Szpirer, J Weissenbach, J-M Claverie and P Avner
A 94 kb genomic sequence 3 to the murine Xist gene reveals an AT rich region containing a new testis specific gene Tsx P. 1713

D W Parsons, P E McAndrew, U R Monani, J R Mendell, A H M Burghes and T W Prior
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene P.1727

R J Wenstrup, G T Langland, M C Willing, V N D'Souza , and W G Cole
A splice-junction mutation in the region of COL5A1 that codes for the carboxyl propeptide of proalpha1(V) chains results in the gravis form of the Ehlers-Danlos syndrome (type I) P. 1733

B Levinson, R Conant, R Schnur, S Das, S Packman and J Gitschier
A repeated element in the regulatory region of the MNK gene and its deletion in a patient with occipital horn syndrome P. 1737

R-J Hu, M P Lee, L A Johnson and A P Feinberg
A novel human homologue of yeast nucleosome assembly protein, 65kb centromeric to the p57KIP2 gene is biallelically expressed in fetal and adult tissues P. 1743

M Speek, F Barry and W L Miller
Alternate promoters and alternate splicing of human tenascin-X, a gene with 5 and 3 ends buried in other genes P. 1749

G Cooper, W Amos, D Hoffman and D C Rubinsztein
Network analysis of human Y microsatellite haplotypes P. 1759

M A Jobling, V Samara, A Pandya, N Fretwell, B Bernasconi, R J Mitchell, T Gerelsaikhan, B Dashnyam, A Sajantila, P J Salo, Y Nakahori, C M Disteche, K Thangaraj, L Singh, M H Crawford and C Tyler-Smith
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males P. 1767

J E Parrish, A E Scheuerle, R A Lewis, M L Levy and D L Nelson
Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti Type 2 P. 1777

P J Byrd, P R Cooper, T Stankovic, H S Kullar, G D J Watts, P J Robinson and A M R Taylor
A gene transcribed from the bidirectional ATM promoter coding for a serine rich protein: amino acid sequence, structure and expression studies P. 1785

C L OKeefe, P E Warburton and A G Matera
Oligonucleotide probes for alpha satellite DNA variants can distinguish homologous chromosomes by FISH P. 1793

F Schnieders, T Dork, J Arnemann, T Vogel, M Werner and J Schmidtke
Testis-specific protein, Y-encoded (TSPY) expression in testicular tissues P. 1801

P Thomas, Y Ye and E Lightner
Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy P. 1809

A Nestorowicz, B A Wilson, K P Schoor, H Inoue, B Glaser, H Landau, C A Stanley, P S Thornton, J P Clement IV, J Bryan, L Aguilar-Bryan and M A Permutt
Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews P. 1813

C A May, A J Jeffreys and J A L Armour
Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309) P. 1823

K Fu, R Hartlen, T Johns, A Genge, G Karpati and E A Shoubridge
A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy P. 1835

E M McNally, D Duggan, J R Gorospe, C G Bonneman, M Fanin, E Pegoraro, H G W Lidov, S Noguchi, E Ozawa, R S Finkel, R P Cruse, C Angelini, L M Kunkel and E P Hoffman

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy P. 1841

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 November 1996 issue, which is shortly to be printed. Copies are scheduled for despatch to subscribers on 20 October 1996.

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.

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