High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation.

Comparative genomic hybridization array study and its utility in detection of constitutional and acquired anomalies

Andrieux, Joris
Sheth, Frenny

October 2009

779-791The last decade has witnessed an upsurge in the knowledge of cytogenetic disorders and putti...

Diagnosis of human sub-telomeric chromosomal deletions by Microarray

Darmanian, Artur Pavlovich, Biotechnology & Biomolecular Sciences, Faculty of Science, UNSW

January 2008

ABSTRACTA major cause of genetic disease is associated with chromosomal imbalances, such as deletion...

RESEARCH ARTICLE High Resolution Genomic Analysis of 18q Using Oligo-Microarray Comparative Genomic Hybridization (aCGH)

Patricia L. Heard
Erika M. Carter
Analisa C. Cr
Courtney Sebold
Daniel E. Hale
Jannine D. Cody

January 2009

The advent of oligonucleotide array comparative genomic hy-bridization (aCGH) has revolutionized dia...

Automatic Breakpoint identification and smoothing of array comparative genomic hybridization data

Jong, K.
Marchiori, E.
Meijer, G.J.
Vaart, A.V.D.
Ylstra, B.

January 2004

Contains fulltext : 84530.pdf (publisher's version ) (Closed access)2 p

Whole-genome array comparative genome hybridization: the preferred diagnostic choice in postnatal clinical cytogenetics.

Veltman, J.A.
Vries, B.B. van

January 2007

Contains fulltext : 52059.pdf (publisher's version ) (Closed access

Detection and characterization of chromosomal aberrations in human solid tumors using fluorescence in situ hybridization strategies

Suijkerbuijk, R.F.

January 1994

Contains fulltext : mmubn000001_179492705.pdf (publisher's version ) (Open Access)...

Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

Lugtenberg, D.
Brouwer, A.P.M. de
Kleefstra, T.
Oudakker, A.R.
Frints, S.G.
Schrander-Stumpel, C.T.R.M.
Fryns, J.P.
Jensen, L.R.
Chelly, J.
Moraine, C.
Turner, G.
Veltman, J.A.
Hamel, B.C.J.
Vries, L.B.A. de
Bokhoven, J.H.L.M. van
Yntema, H.G.

January 2006

Contains fulltext : 50912.pdf (publisher's version ) (Closed access)Several studie...

Identification of disease genes by whole genome CGH arrays.

Vissers, L.E.L.M.
Veltman, J.A.
Geurts van Kessel, A.H.M.
Brunner, H.G.

January 2005

Contains fulltext : 47561.pdf (publisher's version ) (Closed access)Small, submicr...

Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.

Kousoulidou, L.
Parkel, S.
Zilina, O.
Palta, P.
Puusepp, H.
Remm, M.
Turner, G.
Boyle, J.
Bokhoven, J.H.L.M. van
Brouwer, A.
Esch, H. van
Froyen, G.
Ropers, H.H.
Chelly, J.
Moraine, C.
Gecz, J.
Kurg, A.
Patsalis, P.C.

January 2007

Contains fulltext : 53054.pdf (publisher's version ) (Closed access)The rapid adva...

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Redin, C.
Brand, H.
Collins, R.
Kammin, T.
Mitchell, E.
Hodge, J.C.
Hanscom, C.
Pillalamarri, V.
Seabra, C.M.
Abbott, M.A.
Abdul-Rahman, O.A.
Aberg, E.
Bongers, E.M.H.F.
Vries, B.B.A. de
Koolen, D.A.
Jongmans, M.C.J.
Marcelis, C.L.M.
Bon, B.W.M. van
Burgt, I. van der
Brunner, H.G.
Leeuw, N. de
et al.

January 2017

Contains fulltext : 169855.pdf (publisher's version ) (Closed access

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3.

Solomon, N.M.
Ross, S.
Morgan, T.
Belsky, J.L.
Hol, F.A.
Karnes, P.
Hopwood, N.J.
Myers, S.E.
Tan, A.
Warne, G.L.
Forrest, S.M.
Thomas, P.Q.

January 2004

Contains fulltext : 58319.pdf (publisher's version ) (Closed access)INTRODUCTION: ...

High-resolution genomic microarrays for X-linked mental retardation.

Lugtenberg, D.
Veltman, J.A.
Bokhoven, J.H.L.M. van

January 2007

Contains fulltext : 52697.pdf (publisher's version ) (Closed access)Developments i...

High resolution microarray comparatve genomic hybridisation analysis using spotted oligonucleotides

Carvalho, B.
Ouwerkerk, E.
Meijer, G. A.
Ylstra, B.

June 2004

Background: Currently, comparative genomic hybridisation array (array CGH) is the method of choice f...

Development of a high-resolution array of chromosome 1p and its application to the identification of genetic alterations in cancer

Henderson, Laura-Jane Walker

January 2004

Genetic alterations such as deletions, amplifications, and translocations occurring on human chromos...

Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization

Korn, W.M.
Olde Weghuis, D.E.M.
Suijkerbuijk, R.F.
Schmidt, U.
Otto, T.
Manoir, S. du
Geurts van Kessel, A.H.M.
Harstrick, A.
Seeber, S.
Becher, H.

January 1996

Contains fulltext : 23683___.PDF (publisher's version ) (Open Access

Comparative genomic hybridization array study and its utility in detection of constitutional and acquired anomalies

Andrieux, Joris
Sheth, Frenny

October 2009

779-791The last decade has witnessed an upsurge in the knowledge of cytogenetic disorders and putti...

Diagnosis of human sub-telomeric chromosomal deletions by Microarray

Darmanian, Artur Pavlovich, Biotechnology & Biomolecular Sciences, Faculty of Science, UNSW

January 2008

ABSTRACTA major cause of genetic disease is associated with chromosomal imbalances, such as deletion...

RESEARCH ARTICLE High Resolution Genomic Analysis of 18q Using Oligo-Microarray Comparative Genomic Hybridization (aCGH)

Patricia L. Heard
Erika M. Carter
Analisa C. Cr
Courtney Sebold
Daniel E. Hale
Jannine D. Cody

January 2009

The advent of oligonucleotide array comparative genomic hy-bridization (aCGH) has revolutionized dia...

Automatic Breakpoint identification and smoothing of array comparative genomic hybridization data

Jong, K.
Marchiori, E.
Meijer, G.J.
Vaart, A.V.D.
Ylstra, B.

January 2004

Contains fulltext : 84530.pdf (publisher's version ) (Closed access)2 p

Whole-genome array comparative genome hybridization: the preferred diagnostic choice in postnatal clinical cytogenetics.

Veltman, J.A.
Vries, B.B. van

January 2007

Contains fulltext : 52059.pdf (publisher's version ) (Closed access

Detection and characterization of chromosomal aberrations in human solid tumors using fluorescence in situ hybridization strategies

Suijkerbuijk, R.F.

January 1994

Contains fulltext : mmubn000001_179492705.pdf (publisher's version ) (Open Access)...

Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

Lugtenberg, D.
Brouwer, A.P.M. de
Kleefstra, T.
Oudakker, A.R.
Frints, S.G.
Schrander-Stumpel, C.T.R.M.
Fryns, J.P.
Jensen, L.R.
Chelly, J.
Moraine, C.
Turner, G.
Veltman, J.A.
Hamel, B.C.J.
Vries, L.B.A. de
Bokhoven, J.H.L.M. van
Yntema, H.G.

January 2006

Contains fulltext : 50912.pdf (publisher's version ) (Closed access)Several studie...

Identification of disease genes by whole genome CGH arrays.

Vissers, L.E.L.M.
Veltman, J.A.
Geurts van Kessel, A.H.M.
Brunner, H.G.

January 2005

Contains fulltext : 47561.pdf (publisher's version ) (Closed access)Small, submicr...

Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.

Kousoulidou, L.
Parkel, S.
Zilina, O.
Palta, P.
Puusepp, H.
Remm, M.
Turner, G.
Boyle, J.
Bokhoven, J.H.L.M. van
Brouwer, A.
Esch, H. van
Froyen, G.
Ropers, H.H.
Chelly, J.
Moraine, C.
Gecz, J.
Kurg, A.
Patsalis, P.C.

January 2007

Contains fulltext : 53054.pdf (publisher's version ) (Closed access)The rapid adva...

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Redin, C.
Brand, H.
Collins, R.
Kammin, T.
Mitchell, E.
Hodge, J.C.
Hanscom, C.
Pillalamarri, V.
Seabra, C.M.
Abbott, M.A.
Abdul-Rahman, O.A.
Aberg, E.
Bongers, E.M.H.F.
Vries, B.B.A. de
Koolen, D.A.
Jongmans, M.C.J.
Marcelis, C.L.M.
Bon, B.W.M. van
Burgt, I. van der
Brunner, H.G.
Leeuw, N. de
et al.

January 2017

Contains fulltext : 169855.pdf (publisher's version ) (Closed access

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3.

Solomon, N.M.
Ross, S.
Morgan, T.
Belsky, J.L.
Hol, F.A.
Karnes, P.
Hopwood, N.J.
Myers, S.E.
Tan, A.
Warne, G.L.
Forrest, S.M.
Thomas, P.Q.

January 2004

Contains fulltext : 58319.pdf (publisher's version ) (Closed access)INTRODUCTION: ...

High-resolution genomic microarrays for X-linked mental retardation.

Lugtenberg, D.
Veltman, J.A.
Bokhoven, J.H.L.M. van

January 2007

Contains fulltext : 52697.pdf (publisher's version ) (Closed access)Developments i...

High resolution microarray comparatve genomic hybridisation analysis using spotted oligonucleotides

Carvalho, B.
Ouwerkerk, E.
Meijer, G. A.
Ylstra, B.

June 2004

Background: Currently, comparative genomic hybridisation array (array CGH) is the method of choice f...

Development of a high-resolution array of chromosome 1p and its application to the identification of genetic alterations in cancer

Henderson, Laura-Jane Walker

January 2004

Genetic alterations such as deletions, amplifications, and translocations occurring on human chromos...

Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization

Korn, W.M.
Olde Weghuis, D.E.M.
Suijkerbuijk, R.F.
Schmidt, U.
Otto, T.
Manoir, S. du
Geurts van Kessel, A.H.M.
Harstrick, A.
Seeber, S.
Becher, H.

January 1996

Contains fulltext : 23683___.PDF (publisher's version ) (Open Access

Comparative genomic hybridization array study and its utility in detection of constitutional and acquired anomalies

Andrieux, Joris
Sheth, Frenny

October 2009

779-791The last decade has witnessed an upsurge in the knowledge of cytogenetic disorders and putti...

Diagnosis of human sub-telomeric chromosomal deletions by Microarray

Darmanian, Artur Pavlovich, Biotechnology & Biomolecular Sciences, Faculty of Science, UNSW

January 2008

ABSTRACTA major cause of genetic disease is associated with chromosomal imbalances, such as deletion...

RESEARCH ARTICLE High Resolution Genomic Analysis of 18q Using Oligo-Microarray Comparative Genomic Hybridization (aCGH)

Patricia L. Heard
Erika M. Carter
Analisa C. Cr
Courtney Sebold
Daniel E. Hale
Jannine D. Cody

January 2009

The advent of oligonucleotide array comparative genomic hy-bridization (aCGH) has revolutionized dia...

High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation.

Abstract

Extracted data

High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation.

Abstract

Extracted data

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