Search research articles
Contact Us
Filters
Showing results (1-10 of 45) with videos related to
Page
of 5
Sort By:
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
April 1, 1996
A heritable folate-sensitive fragile site on chromosome 2p 11.2 (FRA2L)
S Schuffenhauer, G Lederer, J Murken
Genomics
|
July 1, 1995
Cyclophilin A, the major intracellular receptor for the immunosuppressant cyclosporin A, maps to chromosome 7p11.2-p13: four pseudogenes map to chromosomes 3, 10, 14, and 18
W Willenbrink, J Halaschek, S Schuffenhauer, et al.
Chromosoma
|
October 2, 2002
A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction
D F Callen, H Eyre, S McDonnell, et al.
Genomics
|
August 10, 1995
The gene coding for glial cell line derived neurotrophic factor (GDNF) maps to chromosome 5p12-p13.1
D Schindelhauer, S Schuffenhauer, T Gasser, et al.
Cytogenetics and Cell Genetics
|
March 11, 1999
Assignment of the human genes coding for cytochrome c oxidase subunits Va (COX5A), VIc (COX6C) and VIIc (COX7C) to chromosome bands 15q25, 8q22-->q23 and 5q14 and of three pseudogenes (COX5AP1, COX6CP1, COX7CP1) to 14q22, 16p12 and 13q14-->q21 by FISH and radiation hybrid mapping
S Hofmann, P Lichtner, S Schuffenhauer, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
April 1, 1994
[Dyskeratosis congenita in monozygous twins]
D Burkhardt, C G Schirren, S Schuffenhauer, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
March 1, 1993
[Incontinentia pigmenti in a male patient]
D Burkhardt, S Schuffenhauer, R U Peter, et al.
Clinical Genetics
|
March 29, 2000
Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery
S von Gernet, A Golla, Y Ehrenfels, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1996
Molecular analysis of an extra inv dup(15)(q13) chromosome in two patients with Angelman syndrome
T Buchholz, S Schuffenhauer, K Evans, et al.
Journal of Medical Genetics
|
January 14, 2000
An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14
P Lichtner, R König, T Hasegawa, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
April 1, 1996
A heritable folate-sensitive fragile site on chromosome 2p 11.2 (FRA2L)
S Schuffenhauer, G Lederer, J Murken
Genomics
|
July 1, 1995
Cyclophilin A, the major intracellular receptor for the immunosuppressant cyclosporin A, maps to chromosome 7p11.2-p13: four pseudogenes map to chromosomes 3, 10, 14, and 18
W Willenbrink, J Halaschek, S Schuffenhauer, et al.
Chromosoma
|
October 2, 2002
A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction
D F Callen, H Eyre, S McDonnell, et al.
Genomics
|
August 10, 1995
The gene coding for glial cell line derived neurotrophic factor (GDNF) maps to chromosome 5p12-p13.1
D Schindelhauer, S Schuffenhauer, T Gasser, et al.
Cytogenetics and Cell Genetics
|
March 11, 1999
Assignment of the human genes coding for cytochrome c oxidase subunits Va (COX5A), VIc (COX6C) and VIIc (COX7C) to chromosome bands 15q25, 8q22-->q23 and 5q14 and of three pseudogenes (COX5AP1, COX6CP1, COX7CP1) to 14q22, 16p12 and 13q14-->q21 by FISH and radiation hybrid mapping
S Hofmann, P Lichtner, S Schuffenhauer, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
April 1, 1994
[Dyskeratosis congenita in monozygous twins]
D Burkhardt, C G Schirren, S Schuffenhauer, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
March 1, 1993
[Incontinentia pigmenti in a male patient]
D Burkhardt, S Schuffenhauer, R U Peter, et al.
Clinical Genetics
|
March 29, 2000
Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery
S von Gernet, A Golla, Y Ehrenfels, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1996
Molecular analysis of an extra inv dup(15)(q13) chromosome in two patients with Angelman syndrome
T Buchholz, S Schuffenhauer, K Evans, et al.
Journal of Medical Genetics
|
January 14, 2000
An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14
P Lichtner, R König, T Hasegawa, et al.
Page
of 5