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Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay

PloS one, 2017-07, Vol.12 (7), p.e0180984-e0180984

2017

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Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR

The Journal of molecular diagnostics : JMD, 2021-08, Vol.23 (8), p.941-951

2021

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BMP4 was associated with NSCL/P in an Asian population

PloS one, 2012-04, Vol.7 (4), p.e35347-e35347

2012

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Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single‐tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta‐thalassemia

Electrophoresis, 2015-12, Vol.36 (23), p.2914-2924

2015

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Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy

Frontiers in genetics, 2019-11, Vol.10, p.1105-1105

2019

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FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

Expert reviews in molecular medicine, 2017-07, Vol.19, p.e10-e10, Article e10

2017

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Germline transgenesis of zebrafish using the medaka Tol1 transposon system

Developmental dynamics, 2008-09, Vol.237 (9), p.2466-2474

2008

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Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay

American journal of hematology, 2015-09, Vol.90 (9), p.E194-E196

2015

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Phylogenetic and evolutionary relationships and developmental expression patterns of the zebrafish twist gene family

Development genes and evolution, 2009-06, Vol.219 (6), p.289-300

2009

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Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome

Prenatal diagnosis, 2015-06, Vol.35 (6), p.534-543

2015

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Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations

European journal of human genetics : EJHG, 2013-12, Vol.21 (12), p.1436-1441

2013

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The FGF and FGFR Gene Family and Risk of Cleft Lip with or Without Cleft Palate

The Cleft palate-craniofacial journal, 2013-01, Vol.50 (1), p.96-103

2013

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Zebrafish twist1 is expressed in craniofacial, vertebral, and renal precursors

Development genes and evolution, 2007-12, Vol.217 (11-12), p.783-789

2007

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Genomic, cDNA, and embryonic expression analysis of zebrafish transforming growth factor beta 3 (tgfβ3)

Developmental dynamics, 2005-04, Vol.232 (4), p.1021-1030

2005

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ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

Chinese medical journal, 2012-02, Vol.125 (3), p.476-480

2012

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Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations

Genetic epidemiology, 2008-09, Vol.32 (6), p.505-512

2008

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tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crest

Mechanisms of development, 2010-07, Vol.127 (7-8), p.329-344

2010

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Rapid and reliable preimplantation genetic diagnosis of common hemoglobin B art's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay

American journal of hematology, 2015-09, Vol.90 (9)

2015

Volltextzugriff (PDF)

Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome: Nonaplex microsatellite PCR panel for Hb Bart's PGD

Prenatal diagnosis, 2015-06, Vol.35 (6), p.534-543

2015

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Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms

Human genetics, 2009-09, Vol.126 (3), p.385-394

2009

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Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations

European journal of human genetics : EJHG, 2009-06, Vol.17 (6), p.831-839

2009

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Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts

American journal of medical genetics. Part A, 2012-04, Vol.158A (4), p.784-794

2012

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Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations

European journal of human genetics : EJHG, 2010-06, Vol.18 (6), p.726-732

2010

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Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay

Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR

BMP4 was associated with NSCL/P in an Asian population

Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single‐tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta‐thalassemia

Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy

FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

Germline transgenesis of zebrafish using the medaka Tol1 transposon system

Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay

Phylogenetic and evolutionary relationships and developmental expression patterns of the zebrafish twist gene family

Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome

Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations

The FGF and FGFR Gene Family and Risk of Cleft Lip with or Without Cleft Palate

Zebrafish twist1 is expressed in craniofacial, vertebral, and renal precursors

Genomic, cDNA, and embryonic expression analysis of zebrafish transforming growth factor beta 3 (tgfβ3)

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations

tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crest

Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate

Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate

Rapid and reliable preimplantation genetic diagnosis of common hemoglobin B art's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay

Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome: Nonaplex microsatellite PCR panel for Hb Bart's PGD

Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms

Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts

Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations

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