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...

Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion

American journal of medical genetics. Part A, 2024-07, p.e63826

2024

Volltextzugriff (PDF)

Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Human reproduction (Oxford), 2023-12, Vol.38 (12), p.2526-2535

2023

Volltextzugriff (PDF)

Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of β-thalassaemia major: Case report

Human reproduction (Oxford), 2005-07, Vol.20 (7), p.1855-1859

2005

Volltextzugriff (PDF)

Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

Obstetrical & gynecological survey, 2024-03, Vol.79 (3), p.164-165

2024

Volltextzugriff (PDF)

Diagnosis and molecular characterization of a novel [alpha]0-thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.e124

2017

Volltextzugriff (PDF)

Diagnosis and molecular characterization of a novel α0‐thalassemia deletion (–Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.e124-e126

2017

Volltextzugriff (PDF)

Two novel variants in theTCF12gene identified in cases with craniosynostosis

Application of clinical genetics, 2019-02, Vol.12, p.19-25

2019

Volltextzugriff (PDF)

Molecular Basis of α-thalassaemia

Thalassemia reports, 2011-12, Vol.1 (12), p.e13

Traeger-Synodinos, J.

2011

Volltextzugriff (PDF)

ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening

Human reproduction (Oxford), 2012-08, Vol.27 (8), p.2569-2569

2012

Volltextzugriff (PDF)

Session 09: ESHRE data reporting on PGD cycles and oocyte donation

Human reproduction (Oxford), 2013-06, Vol.28 (suppl_1), p.i18-i19

2013

Volltextzugriff (PDF)

The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H

British journal of haematology, 1996-01, Vol.92 (2), p.332-335

1996

Volltextzugriff (PDF)

PARAMEDICAL - LABORATORY

Human reproduction (Oxford), 2012-07, Vol.27 (suppl_2), p.ii261-ii263

2012

Volltextzugriff (PDF)

Two new {beta}-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention

Haematologica (Roma), 2009-09, Vol.94 (9), p.1289-1292

2009

Volltextzugriff (PDF)

ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006. Commentary

Human reproduction (Oxford), 2008, Vol.23 (12)

2008

Volltextzugriff (PDF)

Blastocyst biopsy versus cleavage stage biopsy and blastocyst transfer for preimplantation genetic diagnosis of [beta]-thalassaemia: a pilot study

Human reproduction (Oxford), 2007-05, Vol.22 (5), p.1443

2007

Volltextzugriff (PDF)

Reproductive genetics. Pregnancies following blastocyst stage transfer in PGD cycles at risk for [beta]-thalassaemic haemoglobinopathies

Human reproduction (Oxford), 2002-01, Vol.17 (1), p.25

2002

Volltextzugriff (PDF)

O▪71 Six years of PGD for β-haemoglobinopathies and cystic fibrosis in Greece

Reproductive biomedicine online, 2005, Vol.10, p.23-23

2005

Volltextzugriff (PDF)

O▪70 Moving towards blastocyst biopsy: trophectoderm biopsy for PGD of β-thalassaemia

Reproductive biomedicine online, 2005, Vol.10, p.23-23

2005

Volltextzugriff (PDF)

Molecular, haematological and clinical studies of the -- 101 C (right arrow) T substitution of the (beta -globin) gene promoter in 25 (beta -thalassaemia) intermedia patients and 45

British journal of haematology, 1999-12, Vol.107 (4), p.699

1999

Volltextzugriff (PDF)

Molecular, haematological and clinical studies of a silent (beta-gene) C - G mutation at 6bp 3' to the termination codon (+1481 C - G) in twelve Greek families

British journal of haematology, 1998-10, Vol.103 (1), p.45

1998

Volltextzugriff (PDF)

Measurement of the mass of the [tau] lepton

Physical review letters, 1992-11, Vol.69:21

1992

Volltextzugriff (PDF)

Measurement of the mass of the τ lepton

Physical review letters, 1992-11, Vol.69 (21), p.3021-3024

1992

Volltextzugriff (PDF)

A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia

British journal of haematology, 1993-11, Vol.85 (3), p.546-552

1993

Volltextzugriff (PDF)

A widely applicable strategy for single cell genotyping of β-thalassaemia mutations using DGGE analysis : Application to preimplantation genetic diagnosis: Preimplantation Genetics and Diagnosis

Prenatal diagnosis, 1999, Vol.19 (13), p.1209-1216

1999

Volltextzugriff (PDF)

1 – 25 von 60

Suche als RSS-Feed

Aktive Filter

KollektionMEDLINE

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(45)

Publikationsform

Sprache

Englisch
(60)

Erscheinungsjahr

n.n

Thema

Science & Technology
(17)
Life Sciences & Biomedicine
(10)
Biological And Medical Sciences
(8)
Medical Sciences
(8)
Technology
(5)
Aircraft
(4)
Gynecology. Andrology. Obstetrics
(4)
Hematology
(4)
Anemia
(3)
Anemias. Hemoglobinopathies
(3)
Diseases Of Red Blood Cells
(3)
Engineering
(3)
Engineering, Aerospace
(3)
Hematologic And Hematopoietic Diseases
(3)
Obstetrics & Gynecology
(3)
Aircraft Noise
(2)
Airports
(2)
Birth Control
(2)
Exact Sciences And Technology
(2)
Genetics & Heredity
(2)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion

Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL

Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of β-thalassaemia major: Case report

Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

Diagnosis and molecular characterization of a novel [alpha]0-thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Diagnosis and molecular characterization of a novel α0‐thalassemia deletion (–Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Two novel variants in theTCF12gene identified in cases with craniosynostosis

Molecular Basis of α-thalassaemia

ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening

Session 09: ESHRE data reporting on PGD cycles and oocyte donation

The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H

PARAMEDICAL - LABORATORY

Two new {beta}-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention

ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006. Commentary

Blastocyst biopsy versus cleavage stage biopsy and blastocyst transfer for preimplantation genetic diagnosis of [beta]-thalassaemia: a pilot study

Reproductive genetics. Pregnancies following blastocyst stage transfer in PGD cycles at risk for [beta]-thalassaemic haemoglobinopathies

O▪71 Six years of PGD for β-haemoglobinopathies and cystic fibrosis in Greece

O▪70 Moving towards blastocyst biopsy: trophectoderm biopsy for PGD of β-thalassaemia

Molecular, haematological and clinical studies of the -- 101 C (right arrow) T substitution of the (beta -globin) gene promoter in 25 (beta -thalassaemia) intermedia patients and 45

Molecular, haematological and clinical studies of a silent (beta-gene) C - G mutation at 6bp 3' to the termination codon (+1481 C - G) in twelve Greek families

Measurement of the mass of the [tau] lepton

Measurement of the mass of the τ lepton

A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia

A widely applicable strategy for single cell genotyping of β-thalassaemia mutations using DGGE analysis : Application to preimplantation genetic diagnosis: Preimplantation Genetics and Diagnosis

Aktive Filter

Suchergebnisse filtern