Volume 105, Issue 4

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October 1999

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15 articles in this issue

Association of genetic polymorphisms of alcohol-metabolizing enzymes with excessive alcohol consumption in Japanese men
F. Sun
I. Tsuritani
Y. Yamada
Original Investigation 28 August 1999 Pages: 295 - 300
Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products
M. Goto
Y. Yamabe
Y. Furuichi
Original Investigation 14 September 1999 Pages: 301 - 307
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?
M. D’Alessandro
I. Naom
F. Muntoni
Original Investigation 31 August 1999 Pages: 308 - 313
β3-Adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study
A.C. Morrison
F.L. Brancati
E. Boerwinkle
Original Investigation 07 September 1999 Pages: 314 - 319
Characterisation of the human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosis
S.R.F. Twigg
A.O.M. Wilkie
Original Investigation 08 September 1999 Pages: 320 - 326
Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutations
M.J. Osborn
M. Upadhyaya
Original Investigation 10 September 1999 Pages: 327 - 332
Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor gene
C. Cybulski
K. Krzystolik
J. Lubiński
Original Investigation 09 September 1999 Pages: 333 - 336
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes
M. Clementi
P. Forabosco
R. Tenconi
Original Investigation 07 September 1999 Pages: 337 - 342
G130V, a common FRDA point mutation, appears to have arisen from a common founder
M.B. Delatycki
M. Knight
S.M. Forrest
Original Investigation 07 September 1999 Pages: 343 - 346
Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes
C. Féral
M. G. Mattéi
G. Guellaën
Original Investigation 15 September 1999 Pages: 347 - 353
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene
K.R. Bowles
J. Gibson
N.E. Bowles
Original Investigation 26 August 1999 Pages: 354 - 359
Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis
M. Moriguchi
C. Terai
N. Kamatani
Original Investigation 14 September 1999 Pages: 360 - 366
X/Y translocation in a family with Leri-Weill dyschondrosteosis
G. Calabrese
R. Fischetto
G. Palka
Short Report 25 August 1999 Pages: 367 - 368
Erratum to: Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases
Miguel Angel Pujana
Jordi Corral
Tha Ataxia Study Group
Erratum 16 September 1999 Pages: 376 - 376
Erratum to: Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis
Miki Hiraoka
Michael T. Trese
Barkur S. Shastry
Erratum 16 September 1999 Pages: 377 - 377

Volume 105, Issue 4

Association of genetic polymorphisms of alcohol-metabolizing enzymes with excessive alcohol consumption in Japanese men

Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products

Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?

β3-Adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study

Characterisation of the human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosis

Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutations

Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor gene

CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes

G130V, a common FRDA point mutation, appears to have arisen from a common founder

Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes

Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene

Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis

X/Y translocation in a family with Leri-Weill dyschondrosteosis

Erratum to: Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases

Erratum to: Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis

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