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Diagnostic utility of microarray testing in pregnancy loss

Ultrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.478-486

2015

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Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2

Clinical genetics, 2010-08, Vol.78 (2), p.162-168

2010

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Diagnostic Utility of Microarray Testing in Pregnancy Loss

Obstetrical & gynecological survey, 2016-01, Vol.71 (1), p.15-16

2016

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Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly

Molecular syndromology, 2013-01, Vol.3 (6), p.247-254

2013

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Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems

Genetics in medicine, 2011-10, Vol.13 (10), p.868-880

2011

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The human NTT gene : Identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4+ T cells

Genomics (San Diego, Calif.), 1997-01, Vol.39 (2), p.171-184

1997

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Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1

Molecular syndromology, 2011-05, Vol.1 (5), p.262-271

2011

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Lack of X inactivation associated with maternal X isodisomy : Evidence for a counting mechanism prior to X inactivation during human embryogenesis

American journal of human genetics, 1996, Vol.58 (1), p.161-170

1996

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O4 Mechanisms of lung cancer hyper-progression promoted by PD-1 immune checkpoint blockade

Journal for immunotherapy of cancer, 2020-10, Vol.8 (Suppl 2), p.A5-A5

2020

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Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis

Genetics in medicine, 2012-11, Vol.14 (11), p.914-921

2012

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NF1 microduplications: identification of seven nonrelated individuals provides further characterization of the phenotype

Genetics in medicine, 2012-05, Vol.14 (5), p.508-514

2012

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Diagnostic utility of microarray testing in pregnancy loss: Microarray and fetal loss

Ultrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.478-486

2015

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Floating photocatalysts based on TiO2 supported on high surface area exfoliated vermiculite for water decontamination

Catalysis communications, 2006-08, Vol.7 (8), p.538-541

2006

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Region-specific FISH probes used to identify and characterize an interstitial paracentric inv(21)(q22.1q22.3)

Prenatal diagnosis, 1998-08, Vol.18 (8), p.849-853

1998

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DNA replication analysis of FMRI, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late

American journal of human genetics, 1994-07, Vol.55 (1), p.96-104

1994

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Molecular Characterization of Tiny Ring X Chromosomes from Females with Functional X Chromosome Disomy and Lack of cis X Inactivation

Genomics (San Diego, Calif.), 1995-05, Vol.27 (1), p.182-188

1995

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Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories

Genetics in medicine, 2009-12, Vol.11 (12), p.866-873

2009

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Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodeveiopmental disorders

Genetics in medicine, 2010-11, Vol.12 (11), p.694-702

2010

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DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late

American journal of human genetics, 1994-07, Vol.55 (1), p.96-104

1994

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The XIST locus replicates late on the active X, and earlier on the inactive X based on FISH DNA replication analysis of somatic cell hybrids

Somatic cell and molecular genetics, 1995-09, Vol.21 (5), p.327-333

1995

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Perioperative assessment of coagulability in neurosurgical patients using thromboelastography

Surgical neurology, 2002-07, Vol.58 (1), p.5-11

2002

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Floating photocatalysts based on TiO 2 supported on high surface area exfoliated vermiculite for water decontamination

Catalysis communications, 2006, Vol.7 (8), p.538-541

2006

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XIST expression is repressed when X inactivation is reversed in human placental cells: a model for study of XIST regulation

Somatic cell and molecular genetics, 1995-01, Vol.21 (1), p.51-60

1995

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The human NTT gene: Identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4 super(+) T cells

Genomics (San Diego, Calif.), 1997-01, Vol.39 (2), p.171-184

1997

Volltextzugriff (PDF)

Molecular characterization of tiny ring X chromosomes from females with function X chromosome disomy and lack of cis X inactivation

Genomics (San Diego, Calif.), 1995, Vol.27 (1), p.182-188

1995

Volltextzugriff (PDF)

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Diagnostic utility of microarray testing in pregnancy loss

Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2

Diagnostic Utility of Microarray Testing in Pregnancy Loss

Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems

The human NTT gene : Identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4+ T cells

Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1

Lack of X inactivation associated with maternal X isodisomy : Evidence for a counting mechanism prior to X inactivation during human embryogenesis

O4 Mechanisms of lung cancer hyper-progression promoted by PD-1 immune checkpoint blockade

Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis

NF1 microduplications: identification of seven nonrelated individuals provides further characterization of the phenotype

Diagnostic utility of microarray testing in pregnancy loss: Microarray and fetal loss

Floating photocatalysts based on TiO2 supported on high surface area exfoliated vermiculite for water decontamination

Region-specific FISH probes used to identify and characterize an interstitial paracentric inv(21)(q22.1q22.3)

DNA replication analysis of FMRI, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late

Molecular Characterization of Tiny Ring X Chromosomes from Females with Functional X Chromosome Disomy and Lack of cis X Inactivation

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodeveiopmental disorders

DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late

The XIST locus replicates late on the active X, and earlier on the inactive X based on FISH DNA replication analysis of somatic cell hybrids

Perioperative assessment of coagulability in neurosurgical patients using thromboelastography

Floating photocatalysts based on TiO 2 supported on high surface area exfoliated vermiculite for water decontamination

XIST expression is repressed when X inactivation is reversed in human placental cells: a model for study of XIST regulation

The human NTT gene: Identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4 super(+) T cells

Molecular characterization of tiny ring X chromosomes from females with function X chromosome disomy and lack of cis X inactivation

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