Volume 22 Issue 2, June 1999

Chips for chimps

• Andrew G Clark

Creating deaths from malaria

• Mats Wahlgren

You give me fever

• David Valle

Touching base

A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans

• John C. Achermann
• Masafumi Ito
• J. Larry Jameson

Cloning of male mice from adult tail-tip cells

• Teruhiko Wakayama
• Ryuzo Yanagimachi

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

• Julian Zielenski
• Mary Corey
• Lap-Chee Tsui

An estimated frequency of endogenous insertional mutations in humans

• Haig H. Kazazian Jr

Imprinting and monogamy

• Tom Moore
• Walter Mills

Genetic conflicts and the private life of Peromyscus polionotus

• David Haig

The future of genetic counselling: an international perspective

• Barbara Bowles Biesecker
• Theresa M. Marteau

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

• L Kruglyak

A polymorphism that affects OCT-1 binding to the TNF promoter region is associated with severe malaria

• Julian C. Knight
• Irina Udalova
• Dominic Kwiatkowski

Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter

• Jose A. Camacho
• Cassandra Obie
• David Valle

The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

• Keiko Kobayashi
• David S. Sinasac
• Takeyori Saheki

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays

• Joseph G. Hacia
• Jian-Bing Fan
• Francis S. Collins

Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment

• Jeffrey M. Drazen
• Chandri N. Yandava
• Jeffrey Drajesk

A double-stranded RNA binding protein required for activation of repressed messages in mammalian germ cells

• Jun Zhong
• Antoine H.F.M. Peters
• Robert E. Braun

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

• Sander M. Houten
• Wietse Kuis
• Bwee Tien Poll-The

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome

• Joost P.H. Drenth
• Laurence Cuisset
• Marc Delpech & contributing members of the International Hyper-IgD Study Group

The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase

• Xiao Yu Liu
• Andrew W. Dangel
• Gail E. Herman

Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus

• Hiroyuki Yamamoto
• András Simon
• Thaddeus P. Dryja

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

• Eric Delpire
• Jianming Lu
• Tina Thorne

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

• Deeann E. Wallis
• Erich Roessler
• Maximilian Muenke

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

• Edwin M. Stone
• Andrew J. Lotery
• Daniel F. Schorderet

DNA methylation represses transcription in vivo

• Zahava Siegfried
• Sharon Eden
• Howard Cedar

Summer array

Erratum: Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome

• Bruce T Lahn
• David C Page

Erratum: Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells

• Bradford Coffee
• et al.