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Clinical Genetics|August 1, 1987
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6H Eiberg, D Bixler, L S Nielsen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1alpha gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probandsS A Urhammer, T Hansen, C T Ekstrøm, et al.
Psychiatric Genetics|January 1, 1995
A possible locus for manic depressive illness on chromosome 16p13H Ewald, O Mors, T Flint, et al.
American Journal of Medical Genetics|October 9, 1995
Linkage analysis between manic-depressive illness and markers on the long arm of chromosome 11H Ewald, O Mors, T Flint, et al.
Ugeskrift for Laeger|March 30, 1992
[Preclinical and prenatal diagnosis of familial adenomatous polyposis]M L Bisgaard, S Bülow, K Winther, et al.
Scandinavian Journal of Urology and Nephrology. Supplementum|January 1, 1997
Clinical enuresis phenotypes in familial nocturnal enuresisA von Gontard, E Hollmann, H Eiberg, et al.
Human Molecular Genetics|February 1, 1994
Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3A Gal, S Xu, Y Piczenik, et al.
Clinical Genetics|June 22, 2010
RUNX2 analysis of Danish cleidocranial dysplasia familiesL Hansen, A K Riis, A Silahtaroglu, et al.
Diabetes|April 2, 1999
Intermediate expansions of a GAA repeat in the frataxin gene are not associated with type 2 diabetes or altered glucose-induced beta-cell function in Danish CaucasiansL T Dalgaard, T Hansen, S A Urhammer, et al.
Glycobiology|June 11, 1998
Genomic organization and chromosomal localization of three members of the UDP-N-acetylgalactosamine: polypeptide N-acetylgalactosaminyltransferase familyE P Bennett, D O Weghuis, G Merkx, et al.
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