UB Paderborn / Katalog / Suche / in CDI

1 – 21 von 21

Sortiert nach

A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2

Cytogenetic and genome research, 2018-01, Vol.156 (1), p.5-8

2018

Volltextzugriff (PDF)

Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2984-2987

2016

Volltextzugriff (PDF)

Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns‐like phenotype

Prenatal diagnosis, 2017-06, Vol.37 (6), p.602-610

2017

Volltextzugriff (PDF)

Suitability of Rapid Aneuploidy Detection for Prenatal Diagnosis

Journal of obstetrics and gynaecology Canada, 2008-09, Vol.30 (9), p.781-787

2008

Volltextzugriff (PDF)

Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling

Prenatal diagnosis, 2009-03, Vol.29 (3), p.283-286

2009

Volltextzugriff (PDF)

Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype: Prenatal diagnosis of mosaic trisomy 1q

Prenatal diagnosis, 2017-06, Vol.37 (6), p.602-610

2017

Volltextzugriff (PDF)

Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis

Clinical dysmorphology, 2007-10, Vol.16 (4), p.253

2007

Volltextzugriff (PDF)

Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1

Human genetics, 1994-02, Vol.93 (2), p.135-138

1994

Volltextzugriff (PDF)

Effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm

Molecular reproduction and development, 1991-10, Vol.30 (2), p.159-163

1991

Volltextzugriff (PDF)

A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2

Cytogenetic and genome research, 2018, Vol.156 (1), p.5-8

2018

Volltextzugriff (PDF)

Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier

Clinical genetics, 1992-05, Vol.41 (5), p.266-269

1992

Volltextzugriff (PDF)

The effects of cryopreservation on the frequency and type of chromosome abnormalities in human sperm

Chernos, Judy E

1988

Volltextzugriff (PDF)

An investigation of human sperm pronuclear chromosome "gaps" using scanning electron microscopy

Cytogenetics and cell genetics, 1986-01, Vol.42 (1-2), p.57

1986

Volltextzugriff (PDF)

Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome

American journal of human genetics, 2005-05, Vol.76 (5), p.865-876

2005

Volltextzugriff (PDF)

A Comparison of the Frequency of Sperm Chromosome Abnormalities in Men with Mild, Moderate, and Severe Oligozoospermia

Biology of reproduction, 2003-08, Vol.69 (2), p.535-539

2003

Volltextzugriff (PDF)

A novel method for generating xeno-free human feeder cells for human embryonic stem cell culture

Stem cells and development, 2008-06, Vol.17 (3), p.413

2008

Volltextzugriff (PDF)

Chromosome Abnormalities in Sperm From Infertile Men with Asthenoteratozoospermia

Biology of reproduction, 2002-06, Vol.66 (6), p.1781-1783

2002

Volltextzugriff (PDF)

Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia

Human reproduction (Oxford), 2000-05, Vol.15 (5), p.1121-1124

2000

Volltextzugriff (PDF)

Unusual segregation products in sperm from a pericentric inversion 17 heterozygote

Human genetics, 2005-08, Vol.117 (4), p.357-365

2005

Volltextzugriff (PDF)

Analysis of chromosome segregation in sperm from a chromosome 2 inversion heterozygote and assessment of an interchromosomal effect

American journal of medical genetics, 2004-06, Vol.127A (2), p.139-143

2004

Volltextzugriff (PDF)

Analysis of Aneuploidy in Spermatozoa From Testicular Biopsies From Men With Nonobstructive Azoospermia

Journal of andrology, 2003-01, Vol.24 (1), p.100-103

2003

Volltextzugriff (PDF)

1 – 21 von 21

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(16)

Publikationsform

Sprache

Englisch
(21)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2

Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis

Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns‐like phenotype

Suitability of Rapid Aneuploidy Detection for Prenatal Diagnosis

Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling

Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype: Prenatal diagnosis of mosaic trisomy 1q

Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis

Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1

Effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm

A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2

Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier

The effects of cryopreservation on the frequency and type of chromosome abnormalities in human sperm

An investigation of human sperm pronuclear chromosome "gaps" using scanning electron microscopy

Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome

A Comparison of the Frequency of Sperm Chromosome Abnormalities in Men with Mild, Moderate, and Severe Oligozoospermia

A novel method for generating xeno-free human feeder cells for human embryonic stem cell culture

Chromosome Abnormalities in Sperm From Infertile Men with Asthenoteratozoospermia

Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia

Unusual segregation products in sperm from a pericentric inversion 17 heterozygote

Analysis of chromosome segregation in sperm from a chromosome 2 inversion heterozygote and assessment of an interchromosomal effect

Analysis of Aneuploidy in Spermatozoa From Testicular Biopsies From Men With Nonobstructive Azoospermia

Suchergebnisse filtern