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Dive into the research topics where de la Chapelle A is active.

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Featured researches published by de la Chapelle A.


American Journal of Human Genetics | 2003

2002 William Allan Award Address. Inherited human diseases: victories, challenges, disappointments.

de la Chapelle A

More than 1,000 disease genes have been cloned and their mutations characterized, including those that account for the most common Mendelian disorders. While this represents one glorious consequence of the global genome initiatives, it also is a mere beginning.Received November 5, 2002; accepted for publicationNovember14, 2002; electronically published January 23, 2003.Address for correspondence and reprints: Dr. Albert de la Cha-pelle, Human Cancer Genetics Program, 646 Tzagournis MedicalResearch Facility, 420 West 12th Avenue, Columbus, OH 43210.E-mail: [email protected]* Previously presented at the annual meeting of The AmericanSociety of Human Genetics, in Baltimore, on October 18, 2002.


American Journal of Human Genetics | 1972

Analytic review: nature and origin of males with XX sex chromosomes.

de la Chapelle A


American Journal of Human Genetics | 1974

Pericentric inversions of human chromosomes 9 and 10.

de la Chapelle A; Schröder J; Stenstrand K; Fellman J; Herva R; Saarni M; Anttolainen I; Tallila I; Tervilä L; Husa L; Tallqvist G; Robson Eb; Cook Pj; Sanger R


American Journal of Human Genetics | 1996

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.

Moisio Al; Pertti Sistonen; Weissenbach J; de la Chapelle A; Peltomäki P


American Journal of Human Genetics | 1984

The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms.

David C. Page; de la Chapelle A


American Journal of Human Genetics | 1985

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

Ingle C; Robert Williamson; de la Chapelle A; Herva R; Haapala K; Gillian P. Bates; Willard Hf; Pearson P; Davies Ke


American Journal of Human Genetics | 1988

Linkage relationships and gene order around the locus for X-linked retinoschisis.

Alitalo T; Forsius H; Kärnä J; Frants Rr; Eriksson Aw; Wood S; Kruse Ta; de la Chapelle A


American Journal of Human Genetics | 1988

Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.

Saviranta P; Lindlöf M; Anna-Elina Lehesjoki; Kalimo H; Lang H; Sonninen; Savontaus Ml; de la Chapelle A


American Journal of Human Genetics | 1976

A large pericentric inversion of human chromosome 8.

Herva R; de la Chapelle A


American Journal of Human Genetics | 1988

The complicated issue of human sex determination.

de la Chapelle A

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Gillian P. Bates

UCL Institute of Neurology

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David C. Page

University of Wisconsin-Madison

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