Proposed guidelines for papers describing DNA polymorphism-disease associations David N. CooperRobert L. NussbaumMichael Krawczak Editorial 13 February 2002 Pages: 207 - 208
Origin and affinities of indigenous Siberian populations as revealed by HLA class II gene frequencies Tatiana S. Uinuk-oolNaoko TakezakiJan Klein Original Investigation 02 February 2002 Pages: 209 - 226
Characterisation of interstitial duplications and triplications of chromosome 15q11–q13 Siân E. RobertsNicholas R. DennisSimon N. Thomas Original Investigation 02 February 2002 Pages: 227 - 234
Identification and characterization of a novel liver-specific enhancer of the human phenylalanine hydroxylase gene Kuan-Ju ChenHung-Kun ChaoTsung-Sheng Su Original Investigation 05 February 2002 Pages: 235 - 243
A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation Tristan F. McMullanJohn A. CrollaDavid O. Robinson Original Investigation 01 February 2002 Pages: 244 - 250
A case of segmental paternal isodisomy of chromosome 14 Karen J. CovelerSam P. YangLisa G. Shaffer Original Investigation 26 February 2002 Pages: 251 - 256
Genetic study of SMA patients without homozygous SMN1 deletions: identification of compound heterozygotes and characterisation of novel intragenic SMN1 mutations Yolanda MartínAna ValeroConcepción Hernández-Chico Original Investigation 08 February 2002 Pages: 257 - 263
CIA30 complex I assembly factor: a candidate for human complex I deficiency? Rolf JanssenJan SmeitinkLambert van den Heuvel Original Investigation 01 February 2002 Pages: 264 - 270
Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation Catherine L. AndersonCarolyn J. Brown Original Investigation 01 February 2002 Pages: 271 - 278
Identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cysts P. LeegwaterP. BoorM. van der Knaap Original Investigation 08 February 2002 Pages: 279 - 283
Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East Hashem ShahinTom WalshMoien Kanaan Original Investigation 08 February 2002 Pages: 284 - 289
Wiley encyclopedia of molecular medicine David N. Cooper Book Review 06 February 2002 Pages: 291 - 292