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...

Processing and CD3+/CD19+ depletion of cadaveric vertebral bone marrow for primary immunodeficiency patients undergoing sequential bilateral orthotopic lung transplant (BOLT) and bone marrow transplant (BMT)

Cytotherapy (Oxford, England), 2019-05, Vol.21 (5), p.e3-e4

2019

Volltextzugriff (PDF)

Immunity and tolerance after bilateral orthotopic lung transplant (BOLT) in tandem with a CD3+/CD19+ depleted vertebral bone marrow transplant (BOLT+BMT) from 1 of 8 HLA-matched cadaveric donors

Cytotherapy (Oxford, England), 2018-05, Vol.20 (5), p.S118-S119

2018

Volltextzugriff (PDF)

Demonstration of Atmospheric-Pressure Radiometer With Nanocardboard Vanes

Journal of microelectromechanical systems, 2020-10, Vol.29 (5), p.811-817

2020

Volltextzugriff (PDF)

Microfabricated Foldable Wings for Centimeter-Scale Microflyers

Journal of microelectromechanical systems, 2020-10, Vol.29 (5), p.1127-1129

2020

Volltextzugriff (PDF)

Evaluation of buffers to optimize thawing of cryopreserved products for regulatory T cell isolation

Cytotherapy (Oxford, England), 2021-05, Vol.23 (5), p.S163-S164

2021

Volltextzugriff (PDF)

Viability of cryopreserved BM progenitor cells stored for more than a decade

Cytotherapy (Oxford, England), 2002-03, Vol.4 (2), p.157-163

2002

Volltextzugriff (PDF)

355 - Immunity and tolerance after bilateral orthotopic lung transplant (BOLT) in tandem with a CD3+/CD19+ depleted vertebral bone marrow transplant (BOLT+BMT) from 1 of 8 HLA-matched cadaveric donors

Cytotherapy (Oxford, England), 2018-05, Vol.20 (5), p.S118-S119

2018

Volltextzugriff (PDF)

Chromosomal localization of the human gene for palmitoyl-CoA ligase (FACL1)

Cytogenetic and genome research, 1992, Vol.59 (1), p.17-19

1992

Volltextzugriff (PDF)

Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation

Journal of medical genetics, 1993-07, Vol.30 (7), p.614-615

1993

Volltextzugriff (PDF)

Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes

Human heredity, 1992, Vol.42 (3), p.172-178

1992

Volltextzugriff (PDF)

Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22-->pter and trisomy 10p11.2-->pter and 11q21 analysed by dual and triple colour FISH

Journal of medical genetics, 1997-08, Vol.34 (8), p.696-699

1997

Volltextzugriff (PDF)

Paracentric inversion inv(18)(q21.1q23) in a woman with recurrent spontaneous abortions

American journal of medical genetics, 1990-04, Vol.35 (4), p.592-593

1990

Volltextzugriff (PDF)

Triple structural moisaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation

Journal of medical genetics, 1993, Vol.30 (7), p.614-615

1993

Volltextzugriff (PDF)

Supernumerary marker chromosomes characterized by fluorescence in situ hybridization (FISH)

Journal of applied genetics, 1996-01, Vol.37 (3), p.313-324

1996

Volltextzugriff (PDF)

Identification of three different chromosomal additions by chromosome painting using fluorescence in situ hybridization (FISH) technique

Journal of applied genetics, 1996-01, Vol.37 (2), p.197-204

1996

Volltextzugriff (PDF)

Molecular versus classical cytogenetics - Evaluation of 20 Prader-Willi syndrome patients

Journal of applied genetics, 1997-01, Vol.38 (2), p.217-226

1997

Volltextzugriff (PDF)

Prenatal diagnosis of chromosomal aberrations in the second trimester of pregnancy--analysis of problems and diagnostic difficulties

Ginekologia polska, 1989-07, Vol.60 (7-9), p.373

1989

Volltextzugriff (PDF)

Paracentric inversion inv(18)(q21.1q23) in a woman with recurrent spontaneous abortions

American journal of medical genetics, 1990, Vol.35 (4), p.592-593

1990

Volltextzugriff (PDF)

Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland: X-Linked mental retardation. Part I

American journal of medical genetics, 1996, Vol.64 (1), p.184-186

1996

Volltextzugriff (PDF)

Cytogenetic studies in clinical diagnosis --analysis of 1611 examination results

Przeglad lekarski, 1995, Vol.52 (1), p.5

1995

Volltextzugriff (PDF)

Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods

Pediatria polska, 1996-03, Vol.71 (3), p.241-245

1996

Volltextzugriff (PDF)

Partial trisomy of chromosome 13--diagnosis confirmed with the FISH in situ hybridization technique

Pediatria polska, 1996-03, Vol.71 (3), p.247-252

1996

Volltextzugriff (PDF)

Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype

Pediatria polska, 1996-03, Vol.71 (3), p.203-209

1996

Volltextzugriff (PDF)

Reliability of cytogenetic and clinical diagnostic studies. Results of analyzing 1621 pre- and postnatal studies

Pediatria polska, 1995-10, Vol.70 (10), p.803-808

1995

Volltextzugriff (PDF)

1 – 25 von 136

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(79)
Mit Volltextzugriff
(98)

Publikationsform

Sprache

Englisch
(112)
Polnisch
(23)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(61)
Technology
(41)
Humans
(37)
Engineering
(33)
Engineering, Electrical & Electronic
(33)
Telecommunications
(32)
Mobile Communication
(29)
Quality Of Service
(29)
Power Control
(27)
Interference
(23)
Female
(21)
Wireless Networks
(20)
Male
(19)
Life Sciences & Biomedicine
(18)
Multiaccess Communication
(18)
Computer Science
(15)
Resource Management
(15)
Wireless Communication
(15)
Adult
(14)
Applied Sciences
(14)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 30 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Processing and CD3+/CD19+ depletion of cadaveric vertebral bone marrow for primary immunodeficiency patients undergoing sequential bilateral orthotopic lung transplant (BOLT) and bone marrow transplant (BMT)

Immunity and tolerance after bilateral orthotopic lung transplant (BOLT) in tandem with a CD3+/CD19+ depleted vertebral bone marrow transplant (BOLT+BMT) from 1 of 8 HLA-matched cadaveric donors

Demonstration of Atmospheric-Pressure Radiometer With Nanocardboard Vanes

Microfabricated Foldable Wings for Centimeter-Scale Microflyers

Evaluation of buffers to optimize thawing of cryopreserved products for regulatory T cell isolation

Viability of cryopreserved BM progenitor cells stored for more than a decade

355 - Immunity and tolerance after bilateral orthotopic lung transplant (BOLT) in tandem with a CD3+/CD19+ depleted vertebral bone marrow transplant (BOLT+BMT) from 1 of 8 HLA-matched cadaveric donors

Chromosomal localization of the human gene for palmitoyl-CoA ligase (FACL1)

Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation

Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes

Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22-->pter and trisomy 10p11.2-->pter and 11q21 analysed by dual and triple colour FISH

Paracentric inversion inv(18)(q21.1q23) in a woman with recurrent spontaneous abortions

Triple structural moisaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation

Supernumerary marker chromosomes characterized by fluorescence in situ hybridization (FISH)

Identification of three different chromosomal additions by chromosome painting using fluorescence in situ hybridization (FISH) technique

Molecular versus classical cytogenetics - Evaluation of 20 Prader-Willi syndrome patients

Prenatal diagnosis of chromosomal aberrations in the second trimester of pregnancy--analysis of problems and diagnostic difficulties

Paracentric inversion inv(18)(q21.1q23) in a woman with recurrent spontaneous abortions

Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland: X-Linked mental retardation. Part I

Cytogenetic studies in clinical diagnosis --analysis of 1611 examination results

Transmission of HIV Drug Resistance and the Predicted Effect on Current First-line Regimens in Europe

Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods

Partial trisomy of chromosome 13--diagnosis confirmed with the FISH in situ hybridization technique

Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype

Reliability of cytogenetic and clinical diagnostic studies. Results of analyzing 1621 pre- and postnatal studies

Suchergebnisse filtern