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American Journal of Medical Genetics
|
September 15, 1992
Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3)
N Tommerup, C B van der Hagen, A Heiberg
American Journal of Medical Genetics
|
May 1, 1988
Screening for the fragile X: how many cells should we analyse?
N Tommerup, S Laing, I J Christensen, et al.
American Journal of Medical Genetics
|
March 27, 1995
Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome
R E Orstavik, N Tommerup, K Eiklid, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 10, 1993
[Gastrointestinal manifestations in neurofibromatosis]
A K Lie, C F Lindboe, N Tommerup, et al.
Hereditas
|
January 1, 1989
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22
K Arheden, U Tantravahi, N Tommerup, et al.
Human Genetics
|
January 1, 1982
Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28)
K B Nielsen, N Tommerup, H V Dyggve, et al.
Cytogenetic and Genome Research
|
August 12, 2004
LNA-modified oligonucleotides are highly efficient as FISH probes
A Silahtaroglu, H Pfundheller, A Koshkin, et al.
Acta Ophthalmologica
|
August 1, 1987
Characterization of an intraocular retinoblastoma-like tumour
J Winther, O A Jensen, J U Prause, et al.
Journal of Medical Genetics
|
November 1, 1993
Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5)
N Tommerup, C A Brandt, S Pedersen, et al.
Genomics
|
September 1, 1996
Assignment of human elongation factor 1alpha genes: EEF1A maps to chromosome 6q14 and EEF1A2 to 20q13.3
A Lund, S M Knudsen, H Vissing, et al.
Page
of 18
Search research articles
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Showing results (51-60 of 179) with videos related to
Sort By:
Page
of 18
American Journal of Medical Genetics
|
September 15, 1992
Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3)
N Tommerup, C B van der Hagen, A Heiberg
American Journal of Medical Genetics
|
May 1, 1988
Screening for the fragile X: how many cells should we analyse?
N Tommerup, S Laing, I J Christensen, et al.
American Journal of Medical Genetics
|
March 27, 1995
Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome
R E Orstavik, N Tommerup, K Eiklid, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 10, 1993
[Gastrointestinal manifestations in neurofibromatosis]
A K Lie, C F Lindboe, N Tommerup, et al.
Hereditas
|
January 1, 1989
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22
K Arheden, U Tantravahi, N Tommerup, et al.
Human Genetics
|
January 1, 1982
Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28)
K B Nielsen, N Tommerup, H V Dyggve, et al.
Cytogenetic and Genome Research
|
August 12, 2004
LNA-modified oligonucleotides are highly efficient as FISH probes
A Silahtaroglu, H Pfundheller, A Koshkin, et al.
Acta Ophthalmologica
|
August 1, 1987
Characterization of an intraocular retinoblastoma-like tumour
J Winther, O A Jensen, J U Prause, et al.
Journal of Medical Genetics
|
November 1, 1993
Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5)
N Tommerup, C A Brandt, S Pedersen, et al.
Genomics
|
September 1, 1996
Assignment of human elongation factor 1alpha genes: EEF1A maps to chromosome 6q14 and EEF1A2 to 20q13.3
A Lund, S M Knudsen, H Vissing, et al.
Page
of 18