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American Journal of Medical Genetics
|
January 1, 1981
Marker X chromosome induction in fibroblasts by FUdR
N 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 6p21.3
H Vissing, L Aagaard, N Tommerup, et al.
Prenatal Diagnosis
|
October 1, 1983
Fragile X demonstrated retrospectively in amniotic cells cultured in low folate medium
L 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 disorders
N Tommerup, Z Tümer, T Tønnesen, et al.
Clinical Genetics
|
February 1, 1993
High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndrome
M 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-->q31.3
M 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----q42.13
P D Sørensen, B Lomholt, S Frederiksen, et al.
Human Genetics
|
January 1, 1982
Apparent homozygosity for the fragile site at Xq28 in a normal female
K B Nielsen, N Tommerup, H Poulsen, et al.
European Journal of Protistology
|
December 1, 2012
Chemotaxis in tetrahymena
P 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 carriers
K B Nielsen, N Tommerup, H Poulsen, et al.
Page
of 18
Search research articles
Search
Showing results (41-50 of 179) with videos related to
Sort By:
Page
of 18
American Journal of Medical Genetics
|
January 1, 1981
Marker X chromosome induction in fibroblasts by FUdR
N 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 6p21.3
H Vissing, L Aagaard, N Tommerup, et al.
Prenatal Diagnosis
|
October 1, 1983
Fragile X demonstrated retrospectively in amniotic cells cultured in low folate medium
L 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 disorders
N Tommerup, Z Tümer, T Tønnesen, et al.
Clinical Genetics
|
February 1, 1993
High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndrome
M 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-->q31.3
M 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----q42.13
P D Sørensen, B Lomholt, S Frederiksen, et al.
Human Genetics
|
January 1, 1982
Apparent homozygosity for the fragile site at Xq28 in a normal female
K B Nielsen, N Tommerup, H Poulsen, et al.
European Journal of Protistology
|
December 1, 2012
Chemotaxis in tetrahymena
P 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 carriers
K B Nielsen, N Tommerup, H Poulsen, et al.
Page
of 18