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N Tommerup

Showing results (41-50 of 179) with videos related to

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American Journal of Medical Genetics|January 1, 1981
Marker X chromosome induction in fibroblasts by FUdRN Tommerup, K B Nielssen, M Mikkelsen
Genomics|December 1, 1994
Localization of the human gene for advanced glycosylation end product-specific receptor (AGER) to chromosome 6p21.3H Vissing, L Aagaard, N Tommerup, et al.
Prenatal Diagnosis|October 1, 1983
Fragile X demonstrated retrospectively in amniotic cells cultured in low folate mediumL B Nielsen, K B Nielsen, N Tommerup
Journal of Medical Genetics|April 1, 1993
A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disordersN Tommerup, Z Tümer, T Tønnesen, et al.
Clinical Genetics|February 1, 1993
High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndromeM Fannemel, R Riise, B Lofterød, et al.
Cytogenetics and Cell Genetics|July 4, 2001
The human hedgehog-interacting protein gene: structure and chromosome mapping to 4q31.21-->q31.3M Bak, C Hansen, K Friis Henriksen, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Fine mapping of human 5S rRNA genes to chromosome 1q42.11----q42.13P D Sørensen, B Lomholt, S Frederiksen, et al.
Human Genetics|January 1, 1982
Apparent homozygosity for the fragile site at Xq28 in a normal femaleK B Nielsen, N Tommerup, H Poulsen, et al.
European Journal of Protistology|December 1, 2012
Chemotaxis in tetrahymenaP Hellung-Larsen, V Leick, N Tommerup, et al.
Human Genetics|January 1, 1981
X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriersK B Nielsen, N Tommerup, H Poulsen, et al.
Pageof 18

Showing results (41-50 of 179) with videos related to

Sort By:
Pageof 18
American Journal of Medical Genetics|January 1, 1981
Marker X chromosome induction in fibroblasts by FUdRN Tommerup, K B Nielssen, M Mikkelsen
Genomics|December 1, 1994
Localization of the human gene for advanced glycosylation end product-specific receptor (AGER) to chromosome 6p21.3H Vissing, L Aagaard, N Tommerup, et al.
Prenatal Diagnosis|October 1, 1983
Fragile X demonstrated retrospectively in amniotic cells cultured in low folate mediumL B Nielsen, K B Nielsen, N Tommerup
Journal of Medical Genetics|April 1, 1993
A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disordersN Tommerup, Z Tümer, T Tønnesen, et al.
Clinical Genetics|February 1, 1993
High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndromeM Fannemel, R Riise, B Lofterød, et al.
Cytogenetics and Cell Genetics|July 4, 2001
The human hedgehog-interacting protein gene: structure and chromosome mapping to 4q31.21-->q31.3M Bak, C Hansen, K Friis Henriksen, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Fine mapping of human 5S rRNA genes to chromosome 1q42.11----q42.13P D Sørensen, B Lomholt, S Frederiksen, et al.
Human Genetics|January 1, 1982
Apparent homozygosity for the fragile site at Xq28 in a normal femaleK B Nielsen, N Tommerup, H Poulsen, et al.
European Journal of Protistology|December 1, 2012
Chemotaxis in tetrahymenaP Hellung-Larsen, V Leick, N Tommerup, et al.
Human Genetics|January 1, 1981
X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriersK B Nielsen, N Tommerup, H Poulsen, et al.
Pageof 18