UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 583

Sortiert nach

Co-nonsolvency of PNiPAM at the transition between solvation mechanisms

Soft matter, 2014-01, Vol.10 (41), p.8288-8295

2014

Volltextzugriff (PDF)

Hydrophobic hydration of poly-N-isopropyl acrylamide: a matter of the mean energetic state of water

Scientific reports, 2014-03, Vol.4 (1), p.4377-4377, Article 4377

2014

Volltextzugriff (PDF)

Anorectal malformations and pregnancy‐related disorders: a registry‐based case–control study in 17 European regions

BJOG : an international journal of obstetrics and gynaecology, 2013-08, Vol.120 (9), p.1066-1074

2013

Volltextzugriff (PDF)

An epidemiological survey of Mycoplasma hominis and Ureaplasma urealyticum in gynaecological outpatients, Rome, Italy

Epidemiology and infection, 2013-12, Vol.141 (12), p.2650-2657

2013

Volltextzugriff (PDF)

An X-ray chamber for in situ structural studies of solvent-mediated nanoparticle self-assembly

Journal of synchrotron radiation, 2013-03, Vol.20 (2), p.306-315

2013

Volltextzugriff (PDF)

Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia

Neurology, 2004-09, Vol.63 (6), p.1108

2004

Volltextzugriff (PDF)

Prenatal genetic counseling referrals for advanced maternal age: still room for improvement

Prenatal diagnosis, 2014-01, Vol.34 (1), p.71-74

2014

Volltextzugriff (PDF)

Bacterial vaginosis and contraceptive methods

International journal of gynecology and obstetrics, 2000-09, Vol.70 (3), p.341-346

2000

Volltextzugriff (PDF)

Congenital Heart Defects: 15 Years of Experience of the Emilia-Romagna Registry (Italy)

European journal of epidemiology, 2003-01, Vol.18 (8), p.773-780

2003

Volltextzugriff (PDF)

Nanoscale structure of surfactant-induced nanoparticle monolayers at the oil-water interface

Soft matter, 2012-12, Vol.8 (45), p.11478-11483

2012

Volltextzugriff (PDF)

Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene

Gene, 2006-03, Vol.370, p.26-33

2006

Volltextzugriff (PDF)

Core–shell nanoparticle monolayers at planar liquid–liquid interfaces: effects of polymer architecture on the interface microstructure

Soft matter, 2013-01, Vol.9 (14), p.3789-3797

2013

Volltextzugriff (PDF)

Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion

Journal of medical genetics, 2003-08, Vol.40 (8), p.e100-100

2003

Volltextzugriff (PDF)

Maternal Occupational Risk Factors for Oral Clefts

Scandinavian Journal of Work, Environment ＆ Health, 2000-04, Vol.26 (2), p.137-145

2000

Volltextzugriff (PDF)

Nanoscale structure of surfactant-induced nanoparticle monolayers at the oil–water interface

Soft matter, 2012, Vol.8 (45), p.11478

2012

Volltextzugriff (PDF)

Correction: Co-nonsolvency of PNiPAM at the transition between solvation mechanisms

Soft matter, 2014-10, Vol.1 (44), p.93-94

2014

Volltextzugriff (PDF)

Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report

Human reproduction (Oxford), 2004-05, Vol.19 (5), p.1231-1234

2004

Volltextzugriff (PDF)

International Cooperation and Networking in Genetic Health Care Provision: Issues Arising from the Genetic Services Plan for the Emilia-Romagna Region, Italy

Community genetics, 2005-01, Vol.8 (2), p.122-129

2005

Volltextzugriff (PDF)

Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele

Acta oto-laryngologica, 2004-05, Vol.124 (552), p.29-34

2004

Volltextzugriff (PDF)

Antenatal ultrasound diagnosis of genetic syndromes

Reproductive toxicology (Elmsford, N.Y.), 2007-07, Vol.24 (1), p.63-63

2007

Volltextzugriff (PDF)

Mole maker phenotype: possible narrowing of the candidate region

European journal of human genetics : EJHG, 2000-08, Vol.8 (8), p.641-644

2000

Volltextzugriff (PDF)

Epidemiology of Herpes Simplex Virus Infection in Pregnancy: A Pilot Study

European journal of inflammation, 2009-09, Vol.7 (3), p.161-168

2009

Volltextzugriff (PDF)

G.P.12.09 Designing of a high density microarray for the definition of the dystrophin gene transcriptome

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.842-842

2007

Volltextzugriff (PDF)

An appropriate diagnostic approach can improve detection of CFTR mutations: the experience in Patients with Classical Form of Cystic Fibrosis coming from an Italian Region with high genetic heterogeneity

Journal of cystic fibrosis, 2009, Vol.8, p.S6-S6

2009

Volltextzugriff (PDF)

Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey

Prenatal diagnosis, 2004-08, Vol.24 (8), p.647-652

2004

Volltextzugriff (PDF)

1 – 25 von 583

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(381)
Mit Volltextzugriff
(383)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

3 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Co-nonsolvency of PNiPAM at the transition between solvation mechanisms

Hydrophobic hydration of poly-N-isopropyl acrylamide: a matter of the mean energetic state of water

Anorectal malformations and pregnancy‐related disorders: a registry‐based case–control study in 17 European regions

An epidemiological survey of Mycoplasma hominis and Ureaplasma urealyticum in gynaecological outpatients, Rome, Italy

An X-ray chamber for in situ structural studies of solvent-mediated nanoparticle self-assembly

Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia

Prenatal genetic counseling referrals for advanced maternal age: still room for improvement

Bacterial vaginosis and contraceptive methods

Congenital Heart Defects: 15 Years of Experience of the Emilia-Romagna Registry (Italy)

Nanoscale structure of surfactant-induced nanoparticle monolayers at the oil-water interface

Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene

Core–shell nanoparticle monolayers at planar liquid–liquid interfaces: effects of polymer architecture on the interface microstructure

Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion

Maternal Occupational Risk Factors for Oral Clefts

Nanoscale structure of surfactant-induced nanoparticle monolayers at the oil–water interface

Correction: Co-nonsolvency of PNiPAM at the transition between solvation mechanisms

Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report

International Cooperation and Networking in Genetic Health Care Provision: Issues Arising from the Genetic Services Plan for the Emilia-Romagna Region, Italy

Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele

Antenatal ultrasound diagnosis of genetic syndromes

Mole maker phenotype: possible narrowing of the candidate region

Epidemiology of Herpes Simplex Virus Infection in Pregnancy: A Pilot Study

G.P.12.09 Designing of a high density microarray for the definition of the dystrophin gene transcriptome

An appropriate diagnostic approach can improve detection of CFTR mutations: the experience in Patients with Classical Form of Cystic Fibrosis coming from an Italian Region with high genetic heterogeneity

Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey

Suchergebnisse filtern