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Cytogenetics and Cell Genetics
|
January 1, 1995
Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3
E Redeker, M Alders, J M Hoovers, et al.
Human Genetics
|
September 1, 1992
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor
A M van den Ouweland, M Verdijk, M M Mannens, et al.
Cytogenetics and Cell Genetics
|
January 1, 1991
Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization
F Speleman, M Mannens, B Redeker, et al.
Human Genetics
|
April 1, 1993
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization
Y Fukushima, J Hoovers, M Mannens, et al.
Human Mutation
|
June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis
C M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
European Journal of Clinical Investigation
|
October 1, 1996
Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families
C A Fijen, R van den Bogaard, M R Daha, et al.
American Journal of Medical Genetics. Part A
|
May 29, 2020
Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency
Eline A Verberne, Sonja Faries, Marcel M A M Mannens, et al.
Journal of Medical Genetics
|
March 19, 2013
High rate of mosaicism in individuals with Cornelia de Lange syndrome
Sylvia A Huisman, Egbert J W Redeker, Saskia M Maas, et al.
Genetic Analysis : Biomolecular Engineering
|
November 1, 1996
The application of microwave denaturation in comparative genomic hybridization
M de Meulemeester, A Vink, M Jakobs, et al.
European Journal of Human Genetics : EJHG
|
February 1, 2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome
Zahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, et al.
Page
of 18
Search research articles
Search
Showing results (11-20 of 172) with videos related to
Sort By:
Page
of 18
Cytogenetics and Cell Genetics
|
January 1, 1995
Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3
E Redeker, M Alders, J M Hoovers, et al.
Human Genetics
|
September 1, 1992
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor
A M van den Ouweland, M Verdijk, M M Mannens, et al.
Cytogenetics and Cell Genetics
|
January 1, 1991
Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization
F Speleman, M Mannens, B Redeker, et al.
Human Genetics
|
April 1, 1993
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization
Y Fukushima, J Hoovers, M Mannens, et al.
Human Mutation
|
June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis
C M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
European Journal of Clinical Investigation
|
October 1, 1996
Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families
C A Fijen, R van den Bogaard, M R Daha, et al.
American Journal of Medical Genetics. Part A
|
May 29, 2020
Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency
Eline A Verberne, Sonja Faries, Marcel M A M Mannens, et al.
Journal of Medical Genetics
|
March 19, 2013
High rate of mosaicism in individuals with Cornelia de Lange syndrome
Sylvia A Huisman, Egbert J W Redeker, Saskia M Maas, et al.
Genetic Analysis : Biomolecular Engineering
|
November 1, 1996
The application of microwave denaturation in comparative genomic hybridization
M de Meulemeester, A Vink, M Jakobs, et al.
European Journal of Human Genetics : EJHG
|
February 1, 2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome
Zahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, et al.
Page
of 18