Concepedia

Bodil Edman Ahlbom

BE

Statistics

Publications

5

Citations

111

H-Index

5

Active since

1995

Affiliations

Uppsala University Hospital(Current)

Karolinska Institutet

Bodil Edman Ahlbom is an author at Uppsala University Hospital specializing in genetic disorders, human genetics, and medical genetics.

Publications per year

1995–2002

5

Publications

5

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

Bodil Edman Ahlbom, Niklas Dahl, PER ZETTERQVIST et al. · Clinical Genetics · 1995 · 34 citations

, , +14

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

Bodil Edman Ahlbom, Muhammad M. Yaqoob, Agne Larsson et al. · Human Genetics · 1997 · 33 citations

, , +14

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

Bodil Edman Ahlbom, R. Sidenvall, Göran Annerén · American Journal of Medical Genetics · 1996 · 21 citations

, , +16

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

Bodil Edman Ahlbom, Peter G. Goetz, Julie R. Korenberg et al. · American Journal of Medical Genetics · 1996 · 12 citations

, , +16

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

Bodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson et al. · Human Genetics · 2002 · 11 citations

, , +11

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