UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

Cytogenetic and genome research, 2013-01, Vol.139 (3), p.158-163

2013

Volltextzugriff (PDF)

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

Cytogenetic and genome research, 2006-01, Vol.112 (1-2), p.23-34

2006

Volltextzugriff (PDF)

Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases

Human reproduction (Oxford), 2009-08, Vol.24 (8), p.2029-2033

2009

Volltextzugriff (PDF)

Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis

Cytogenetic and genome research, 2014-01, Vol.142 (2), p.145-149

2014

Volltextzugriff (PDF)

An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis

Oncogene, 2010-05, Vol.29 (18), p.2659-2671

2010

Volltextzugriff (PDF)

Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia

Molecular syndromology, 2012-09, Vol.3 (3), p.120-130

2012

Volltextzugriff (PDF)

A report of pure 7p duplication syndrome and review of the literature

American journal of medical genetics. Part A, 2006-12, Vol.140A (24), p.2802-2806

2006

Volltextzugriff (PDF)

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level

International journal of molecular medicine, 2008-02, Vol.21 (2), p.189-200

2008

Volltextzugriff (PDF)

Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding

Cytogenetic and genome research, 2006-08, Vol.114 (3-4), p.240-244

2006

Volltextzugriff (PDF)

Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements

Balkan journal of medical genetics, 2011-01, Vol.14 (2), p.13-16

2011

Volltextzugriff (PDF)

Distal partial trisomy 1q: report of two cases and a review of the literature

Prenatal diagnosis, 2007-09, Vol.27 (9), p.865-871

2007

Volltextzugriff (PDF)

Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?

Cytogenetic and genome research, 2011-01, Vol.132 (1-2), p.121-123

2011

Volltextzugriff (PDF)

Neocentric small supernumerary marker chromosomes (sSMC) – three more cases and review of the literature

Cytogenetic and genome research, 2007-01, Vol.118 (1), p.31-37

2007

Volltextzugriff (PDF)

Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review

American journal of medical genetics. Part A, 2007-11, Vol.143A (22), p.2727-2732

2007

Volltextzugriff (PDF)

Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm

Molecular human reproduction, 2007-10, Vol.13 (10), p.751-756

2007

Volltextzugriff (PDF)

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

Cytogenetic and genome research, 2009-01, Vol.124 (1), p.102-105

2009

Volltextzugriff (PDF)

New insights into the evolution of chromosome 1

Cytogenetic and genome research, 2005-01, Vol.108 (1-3), p.217-222

2005

Volltextzugriff (PDF)

Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints

International journal of molecular medicine, 2007-06, Vol.19 (6), p.855-864

2007

Volltextzugriff (PDF)

Common fragile sites: genomic hotspots of DNA damage and carcinogenesis

International Journal of Molecular Sciences, 2012-09, Vol.13 (9), p.11974-11999

2012

Volltextzugriff (PDF)

Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB)

Cytogenetic and genome research, 2001-01, Vol.93 (3-4), p.242-248

2001

Volltextzugriff (PDF)

Small Supernumerary Marker Chromosomes (sSMC) in Patients with a 45,X/46,X,+mar Karyotype – 17 New Cases and a Review of the Literature

Sexual development, 2007-01, Vol.1 (6), p.353-362

2007

Volltextzugriff (PDF)

Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines

Cytogenetic and genome research, 2006-08, Vol.114 (3-4), p.319-324

2006

Volltextzugriff (PDF)

A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences

Cytogenetic and genome research, 2008-08, Vol.121 (3-4), p.286-287

2008

Volltextzugriff (PDF)

Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations

American journal of medical genetics. Part A, 2010-10, Vol.152A (10), p.2661-2663

2010

Volltextzugriff (PDF)

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face

Cytogenetic and genome research, 2006-08, Vol.114 (3-4), p.330-337

2006

Volltextzugriff (PDF)

1 – 25 von 70

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(61)
Mit Volltextzugriff
(58)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(53)
Life Sciences & Biomedicine
(51)
Humans
(45)
Genetics & Heredity
(33)
Female
(23)
In Situ Hybridization, Fluorescence
(23)
Male
(22)
Cell Biology
(21)
Karyotyping
(21)
Chromosome Aberrations
(15)
Chromosome Banding
(15)
Biological And Medical Sciences
(13)
Genetic Markers
(10)
In Situ Hybridization, Fluorescence - Methods
(10)
Medical Sciences
(10)
Phenotype
(10)
Animals
(8)
Chromosome Mapping
(8)
Original Article
(8)
Small Supernumerary Marker Chromosome
(8)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases

Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis

An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis

Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia

A report of pure 7p duplication syndrome and review of the literature

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level

Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding

Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements

Distal partial trisomy 1q: report of two cases and a review of the literature

Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?

Neocentric small supernumerary marker chromosomes (sSMC) – three more cases and review of the literature

Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review

Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

New insights into the evolution of chromosome 1

Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints

Common fragile sites: genomic hotspots of DNA damage and carcinogenesis

Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB)

Small Supernumerary Marker Chromosomes (sSMC) in Patients with a 45,X/46,X,+mar Karyotype – 17 New Cases and a Review of the Literature

Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines

A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences

Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face

Suchergebnisse filtern