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Experimental Cell Research
|
August 1, 1982
Precision-bored microcapillaries for microinjection of nano-litre quantities without precalibration
N Tommerup
Ugeskrift for Laeger
|
April 4, 2000
[Sequencing of the first human chromosome. The Danish Society of Medical Genetics]
N Tommerup
Ugeskrift for Laeger
|
March 27, 1989
[Retinoblastoma: model for heredity and cancer]
N Tommerup
Journal of Medical Genetics
|
December 1, 1992
Constitutional ring chromosomes and tumour suppressor genes
N Tommerup, R Lothe
Genomics
|
May 20, 1995
Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders
N Tommerup, H Vissing
Genomics
|
March 1, 1996
Assignment of human KH-box-containing genes by in situ hybridization: HNRNPK maps to 9q21.32-q21.33, PCBP1 to 2p12-p13, and PCBP2 to 12q13.12-q13.13, distal to FRA12A
N Tommerup, H Leffers
American Journal of Medical Genetics
|
November 1, 1983
A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome
N Tommerup, F Nielsen
Genomics
|
April 1, 1996
Assignment of the human genes encoding 14,3-3 Eta (YWHAH) to 22q12, 14-3-3 zeta (YWHAZ) to 2p25.1-p25.2, and 14-3-3 beta (YWHAB) to 20q13.1 by in situ hybridization
N Tommerup, H Leffers
Clinical Genetics
|
September 8, 2011
Isolated and syndromic forms of congenital anosmia
H G Karstensen, N Tommerup
Placenta
|
July 1, 1985
Identification of triploidy by DA/DAPI staining of trophoblastic interphase nuclei
N Tommerup, L O Vejerslev
Page
of 18
Search research articles
Search
Showing results (11-20 of 179) with videos related to
Sort By:
Page
of 18
Experimental Cell Research
|
August 1, 1982
Precision-bored microcapillaries for microinjection of nano-litre quantities without precalibration
N Tommerup
Ugeskrift for Laeger
|
April 4, 2000
[Sequencing of the first human chromosome. The Danish Society of Medical Genetics]
N Tommerup
Ugeskrift for Laeger
|
March 27, 1989
[Retinoblastoma: model for heredity and cancer]
N Tommerup
Journal of Medical Genetics
|
December 1, 1992
Constitutional ring chromosomes and tumour suppressor genes
N Tommerup, R Lothe
Genomics
|
May 20, 1995
Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders
N Tommerup, H Vissing
Genomics
|
March 1, 1996
Assignment of human KH-box-containing genes by in situ hybridization: HNRNPK maps to 9q21.32-q21.33, PCBP1 to 2p12-p13, and PCBP2 to 12q13.12-q13.13, distal to FRA12A
N Tommerup, H Leffers
American Journal of Medical Genetics
|
November 1, 1983
A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome
N Tommerup, F Nielsen
Genomics
|
April 1, 1996
Assignment of the human genes encoding 14,3-3 Eta (YWHAH) to 22q12, 14-3-3 zeta (YWHAZ) to 2p25.1-p25.2, and 14-3-3 beta (YWHAB) to 20q13.1 by in situ hybridization
N Tommerup, H Leffers
Clinical Genetics
|
September 8, 2011
Isolated and syndromic forms of congenital anosmia
H G Karstensen, N Tommerup
Placenta
|
July 1, 1985
Identification of triploidy by DA/DAPI staining of trophoblastic interphase nuclei
N Tommerup, L O Vejerslev
Page
of 18