B. Ahlbom

Noonan syndrome with café‐au‐lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus

G. Annéren, N. Dahl, P. Zetterqvist, 1995, Clinical genetics.

Genetic and linkage analysis of familial congenital hypothyroidism: exclusion of linkage to the TSH receptor gene

C. Wadelius, G. Annéren, A. Larsson, 1997, Human Genetics.

Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation.

G. Annéren, R. Sidenvall, B. Ahlbom, 1996, American journal of medical genetics.

Severe psychomotor retardation in a boy with a supernumerary derivative chromosome resulting in partial trisomy 21 and partial trisomy 7p.

C. Wadelius, G. Annéren, R. Saalman, 2003, Annales de genetique.

Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism

C. Wadelius, G. Annéren, A. Larsson, 2002, Human Genetics.

Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype.

J. Korenberg, C. Wadelius, L. Zech, 1996, American journal of medical genetics.