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• Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family.

  Hol FA, Geurds MP, Jensson O, Hamel BC, Moore GE, Newton R, Mariman EC. Hol FA, et al. Hum Genet. 1994 Apr;93(4):452-6. doi: 10.1007/BF00201674. Hum Genet. 1994. PMID: 8168816
• X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

  Lagerström-Fermér M, Sundvall M, Johnsen E, Warne GL, Forrest SM, Zajac JD, Rickards A, Ravine D, Landegren U, Pettersson U. Lagerström-Fermér M, et al. Am J Hum Genet. 1997 Apr;60(4):910-6. Am J Hum Genet. 1997. PMID: 9106538 Free PMC article.
• High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

  Van de Vosse E, Van der Bent P, Heus JJ, Van Ommen GJ, Den Dunnen JT. Van de Vosse E, et al. Mamm Genome. 1997 Jul;8(7):497-501. doi: 10.1007/s003359900483. Mamm Genome. 1997. PMID: 9195994
• Refinement of the localisation of the X linked keratosis follicularis spinulosa decalvans (KFSD) gene in Xp22.13-p22.2.

  Oosterwijk JC, van der Wielen MJ, van de Vosse E, Voorhoeve E, Bakker E. Oosterwijk JC, et al. J Med Genet. 1995 Sep;32(9):736-9. doi: 10.1136/jmg.32.9.736. J Med Genet. 1995. PMID: 8544196 Free PMC article.
• Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis.

  Huopaniemi L, Rantala A, Tahvanainen E, de la Chapelle A, Alitalo T. Huopaniemi L, et al. Am J Hum Genet. 1997 May;60(5):1139-49. Am J Hum Genet. 1997. PMID: 9150161 Free PMC article.