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...

45,X/46,XY mosaicism: report of 27 cases

Pediatrics (Evanston), 1999-08, Vol.104 (2 Pt 1), p.304-308

1999

Volltextzugriff (PDF)

Early Pattern of Epilepsy in the Ring Chromosome 20 Syndrome

Epilepsia (Copenhagen), 2006-03, Vol.47 (3), p.543-549

2006

Volltextzugriff (PDF)

Establishment and characterization of a human parathyroid carcinoma derived cell line

Pathology, research and practice, 2015-04, Vol.211 (4), p.332-340

2015

Volltextzugriff (PDF)

Molecular cytogenetic aberrations in autosomal dominant polycystic kidney disease tissue

Journal of the American Society of Nephrology, 2003-02, Vol.14 (2), p.359-366

2003

Volltextzugriff (PDF)

Detection of DNA copy number changes in human endometriosis by comparative genomic hybridization

Human genetics, 1999-11, Vol.105 (5), p.444-451

1999

Volltextzugriff (PDF)

A Peptidase Gene in Chromosome 8q Is Disrupted by A Balanced Translocation in a Duane Syndrome Patient

Investigative ophthalmology & visual science, 2002-12, Vol.43 (12), p.3609-3612

2002

Volltextzugriff (PDF)

DOR-1, A novel CD10+ stromal cell line derived from progressive Langerhans cell histiocytosis of bone

Pediatric Blood & Cancer, 2005-02, Vol.44 (2), p.128-137

2005

Volltextzugriff (PDF)

Pure proximal deletion of chromosome 21 and kyphosis

European journal of medical genetics, 2007-11, Vol.50 (6), p.469-474

2007

Volltextzugriff (PDF)

DOR-1, a novel CD10+ stromal cell line derived from progressive Langerhans cell histiocytosis of bone. Commentary

Pediatric blood & cancer, 2005, Vol.44 (2), p.117-137

2005

Volltextzugriff (PDF)

Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene

Human genetics, 1998-02, Vol.102 (2), p.151-156

1998

Volltextzugriff (PDF)

A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities

Journal of medical genetics, 1996-09, Vol.33 (9), p.767-771

1996

Volltextzugriff (PDF)

Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion

Human genetics, 1995-10, Vol.96 (4), p.464-468

1995

Volltextzugriff (PDF)

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia

Cancer genetics and cytogenetics, 2008-07, Vol.184 (1), p.22-30

2008

Volltextzugriff (PDF)

Molecular cytogenetic aberrations in CD30 + anaplastic large cell lymphoma cell lines

Cancer genetics and cytogenetics, 2002-10, Vol.138 (2), p.95-101

2002

Volltextzugriff (PDF)

Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)

American journal of medical genetics, 1992-03, Vol.42 (5), p.716-719

1992

Volltextzugriff (PDF)

Cellular and genetic constitution of human endometriosis tissues

Journal of the Society for Gynecologic Investigation, 2000-03, Vol.7 (2), p.79-87

2000

Volltextzugriff (PDF)

Influence of immunomodulators on T lymphocyte differentiation in arc patients and resistance to LAV/HTLV III infection

Comparative immunology, microbiology and infectious diseases, 1986, Vol.9 (2), p.263-267

1986

Volltextzugriff (PDF)

Is Rett syndrome a chromosome breakage syndrome?

American journal of medical genetics, 1994-07, Vol.51 (4), p.602-605

1994

Volltextzugriff (PDF)

Gonadal dysgenesis in del(18p) syndrome

American journal of medical genetics, 1995-07, Vol.57 (4), p.598-600

1995

Volltextzugriff (PDF)

Cellular and Genetic Constitution of Human Endometriosis Tissues

Journal of the Society for Gynecologic Investigation, 2000, Vol.7 (2), p.79-87

2000

Volltextzugriff (PDF)

1 – 20 von 20

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(14)
Mit Volltextzugriff
(19)

Publikationsform

Artikel
(19)
Reviews
(1)

Sprache

Englisch
(20)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

45,X/46,XY mosaicism: report of 27 cases

Early Pattern of Epilepsy in the Ring Chromosome 20 Syndrome

Establishment and characterization of a human parathyroid carcinoma derived cell line

Molecular cytogenetic aberrations in autosomal dominant polycystic kidney disease tissue

Detection of DNA copy number changes in human endometriosis by comparative genomic hybridization

A Peptidase Gene in Chromosome 8q Is Disrupted by A Balanced Translocation in a Duane Syndrome Patient

DOR-1, A novel CD10+ stromal cell line derived from progressive Langerhans cell histiocytosis of bone

Pure proximal deletion of chromosome 21 and kyphosis

DOR-1, a novel CD10+ stromal cell line derived from progressive Langerhans cell histiocytosis of bone. Commentary

Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene

A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities

Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia

Molecular cytogenetic aberrations in CD30 + anaplastic large cell lymphoma cell lines

Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)

Cellular and genetic constitution of human endometriosis tissues

Influence of immunomodulators on T lymphocyte differentiation in arc patients and resistance to LAV/HTLV III infection

Is Rett syndrome a chromosome breakage syndrome?

Gonadal dysgenesis in del(18p) syndrome

Cellular and Genetic Constitution of Human Endometriosis Tissues

Suchergebnisse filtern