Two new Rett syndrome families and review of the literature: expanding the knowledge of <it>MECP2 </it>frameshift mutations by Eiklid Kristin L, Fuglsang Kathrine, Duno Morten, Roende Gitte, Ravn Kirstine, Tümer Zeynep, Nielsen Jytte B, Skjeldal Ola H

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Human <it>CCS</it> gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS) by Tommerup Niels, Petersen Michael B, Werdelin Lene, Panas Marios, Gredal Ole, Brondum-Nielsen Karen, Silahtaroglu Asli N, Tümer Zeynep

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Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5q... by Tommerup Niels, Baekgaard Peter, Pedersen Vibeke, Ledaal Paal, Friis Birgitte, Hahnemann Johanne, Hjalgrim Helle, Tümer Zeynep, Sogaard Marie, Cingöz Sultan, Duno Morten, Brondum-Nielsen Karen

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Clinical expression of Menkes disease in females with normal karyotype by Møller Lisbeth, Lenartowicz Malgorzata, Zabot Marie-Therese, Josiane Arnaud, Burglen Lydie, Bennett Chris, Riconda Daniel, Fisher Richard, Janssens Sandra, Mohammed Shehla, Ausems Margreet, Tümer Zeynep, Horn Nina, Jensen Thomas G

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