UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 78

Sortiert nach

Preimplantation Genetic Diagnosis: Prenatal Testing for Embryos Finally Achieving Its Potential

Journal of clinical medicine, 2014-03, Vol.3 (1), p.280-309

Stern, Harvey J

2014

Volltextzugriff (PDF)

The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts

Molecular cytogenetics, 2014-02, Vol.7 (1), p.18-18

2014

Volltextzugriff (PDF)

The effectiveness of flow cytometric sorting of human sperm (MicroSort®) for influencing a child's sex

Reproductive biology and endocrinology, 2014-11, Vol.12 (1), p.106-106

2014

Volltextzugriff (PDF)

Low utilization of prenatal and pre-implantation genetic diagnosis in Huntington disease - risk discounting in preventive genetics

Clinical genetics, 2015-09, Vol.88 (3), p.220-223

2015

Volltextzugriff (PDF)

Non-disclosing preimplantation genetic diagnosis for Huntington disease

Prenatal diagnosis, 2002-06, Vol.22 (6), p.503-507

2002

Volltextzugriff (PDF)

MicroSort separation of X and Y chromosome-bearing sperm: ongoing clinical trial results

Obstetrics and gynecology (New York. 1953), 2003-04, Vol.101 (4), p.S26-S26

2003

Volltextzugriff (PDF)

Sudden neonatal death in carnitine transporter deficiency

The Journal of pediatrics, 1997-08, Vol.131 (2), p.304-305

1997

Volltextzugriff (PDF)

MicroSort Separation of X and Y Chromosome-Bearing Sperm: Ongoing Clinical Trial Results

Obstetrics and gynecology (New York. 1953), 2003-04, Vol.101 (Supplement), p.26

2003

Volltextzugriff (PDF)

Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis

American journal of medical genetics, 2001-04, Vol.99 (4), p.294-302

2001

Volltextzugriff (PDF)

Lactic Acidosis in Paediatrics: Clinical and Laboratory Evaluation

Annals of Clinical Biochemistry, 1994-09, Vol.31 (5), p.410-419

Stern, Harvey J

1994

Volltextzugriff (PDF)

Non-disclosing preimplantation genetic diagnosis for Huntington disease : Preimplantation Genetics and Diagnosis

Prenatal diagnosis, 2002, Vol.22 (6), p.503-507

2002

Volltextzugriff (PDF)

Rapid detection of the Φ508 deletion in cystic fibrosis by Allele specific PCR and electrochemiluminescent detection

Clinical biochemistry, 1995, Vol.28 (4), p.470-473

1995

Volltextzugriff (PDF)

Prolonged survival in pyruvate carboxylase deficiency: Lack of correlation with enzyme activity in cultured fibroblasts

Clinical biochemistry, 1995-02, Vol.28 (1), p.85-89

1995

Volltextzugriff (PDF)

Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia

Pediatrics (Evanston), 1990-04, Vol.85 (4), p.499

1990

Volltextzugriff (PDF)

Pitfalls of Genetic Testing

The New England journal of medicine, 1996-10, Vol.335 (16), p.1235-1237

1996

Volltextzugriff (PDF)

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

Journal of medical genetics, 1992-03, Vol.29 (3), p.184-187

1992

Volltextzugriff (PDF)

Steroid sulfatase gene in XX males

American journal of human genetics, 1990-02, Vol.46 (2), p.369-376

1990

Volltextzugriff (PDF)

Genetic predisposition testing for breast cancer

The cancer journal from Scientific American, 1996-09, Vol.2 (5), p.244

1996

Volltextzugriff (PDF)

New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters

American journal of medical genetics, 1992-08, Vol.43 (6), p.983-988

1992

Volltextzugriff (PDF)

A theory for the chemical mediation of the excitability of the brain, with special reference to natural and drug-induced sleep

Journal of theoretical biology, 1977-06, Vol.66 (4), p.595-652

1977

Volltextzugriff (PDF)

Inhibition by barbituric acid and its derivatives of the enzymes in rat brain which participate in the synthesis of pyrimidine ribotides

Biochemical pharmacology, 1978-03, Vol.27 (5), p.655-665

1978

Volltextzugriff (PDF)

Atelosteogenesis type III: A distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II

American journal of medical genetics, 1990-06, Vol.36 (2), p.183-195

1990

Volltextzugriff (PDF)

Functional connectivity of hippocampal networks in temporal lobe epilepsy

Epilepsia (Copenhagen), 2014-01, Vol.55 (1), p.137-145

2014

Volltextzugriff (PDF)

Long‐term trajectories of self‐reported cognitive function in a cohort of older survivors of breast cancer: CALGB 369901 (Alliance)

Cancer, 2016-11, Vol.122 (22), p.3555-3563

2016

Volltextzugriff (PDF)

Standardization of analysis sets for reporting results from ADNI MRI data

Alzheimer's & dementia, 2013-05, Vol.9 (3), p.332-337

2013

Volltextzugriff (PDF)

1 – 25 von 78

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(71)
Mit Volltextzugriff
(70)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Preimplantation Genetic Diagnosis: Prenatal Testing for Embryos Finally Achieving Its Potential

The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts

The effectiveness of flow cytometric sorting of human sperm (MicroSort®) for influencing a child's sex

Low utilization of prenatal and pre-implantation genetic diagnosis in Huntington disease - risk discounting in preventive genetics

Non-disclosing preimplantation genetic diagnosis for Huntington disease

MicroSort separation of X and Y chromosome-bearing sperm: ongoing clinical trial results

Sudden neonatal death in carnitine transporter deficiency

MicroSort Separation of X and Y Chromosome-Bearing Sperm: Ongoing Clinical Trial Results

Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis

Lactic Acidosis in Paediatrics: Clinical and Laboratory Evaluation

Non-disclosing preimplantation genetic diagnosis for Huntington disease : Preimplantation Genetics and Diagnosis

Rapid detection of the Φ508 deletion in cystic fibrosis by Allele specific PCR and electrochemiluminescent detection

Prolonged survival in pyruvate carboxylase deficiency: Lack of correlation with enzyme activity in cultured fibroblasts

Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia

Pitfalls of Genetic Testing

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

Steroid sulfatase gene in XX males

Genetic predisposition testing for breast cancer

New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters

A theory for the chemical mediation of the excitability of the brain, with special reference to natural and drug-induced sleep

Inhibition by barbituric acid and its derivatives of the enzymes in rat brain which participate in the synthesis of pyrimidine ribotides

Atelosteogenesis type III: A distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II

Functional connectivity of hippocampal networks in temporal lobe epilepsy

Long‐term trajectories of self‐reported cognitive function in a cohort of older survivors of breast cancer: CALGB 369901 (Alliance)

Standardization of analysis sets for reporting results from ADNI MRI data

Suchergebnisse filtern