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...

Syndromic craniosynostosis: from history to hydrogen bonds

Orthodontics & craniofacial research, 2007-05, Vol.10 (2), p.67-81

2007

Volltextzugriff (PDF)

Clinical care in craniofacial microsomia: A review of current management recommendations and opportunities to advance research

American journal of medical genetics. Part C, Seminars in medical genetics, 2013-11, Vol.163C (4), p.271-282

2013

Volltextzugriff (PDF)

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

Nature genetics, 1996-11, Vol.14 (3), p.353-356

1996

Volltextzugriff (PDF)

Mapping Human Telomere Regions with YAC and P1 Clones: Chromosome-Specific Markers for 27 Telomeres Including 149 STSs and 24 Polymorphisms for 14 Proterminal Regions

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.492-506

1996

Volltextzugriff (PDF)

Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects

Journal of medical genetics, 1997-05, Vol.34 (5), p.414-417

1997

Volltextzugriff (PDF)

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

Genetics in medicine, 2010-10, Vol.12 (10), p.641-647

2010

Volltextzugriff (PDF)

VNTR and microsatellite polymorphisms within the subtelomeric region of 7q

American journal of human genetics, 1993-08, Vol.53 (2), p.509-517

1993

Volltextzugriff (PDF)

GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease

American journal of medical genetics, 1999-03, Vol.83 (3), p.201-206

1999

Volltextzugriff (PDF)

Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and proα2 (1) collagen (COL1A2)

Human molecular genetics, 1992-05, Vol.1 (2), p.135-135

1992

Volltextzugriff (PDF)

Linkage of preaxial polydactyly type 2 to 7q36

American journal of medical genetics, 1995-08, Vol.58 (2), p.128-135

1995

Volltextzugriff (PDF)

Aase syndrome: Novel radiographic features

American journal of medical genetics, 1993-02, Vol.45 (4), p.413-415

1993

Volltextzugriff (PDF)

New Scaphocephaly Severity Indices of Sagittal Craniosynostosis: A Comparative Study with Cranial Index Quantifications

The Cleft palate-craniofacial journal, 2006-03, Vol.43 (2), p.211-221

2006

Volltextzugriff (PDF)

A lethal syndrome resembling branchio-oculo facial syndrome

Clinical genetics, 1992-02, Vol.41 (2), p.74-78

1992

Volltextzugriff (PDF)

Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations

Birth defects research. A Clinical and molecular teratology, 2006-02, Vol.76 (2), p.78-85

2006

Volltextzugriff (PDF)

MDCT diagnosis of the child with posterior plagiocephaly

American journal of roentgenology (1976), 2005-11, Vol.185 (5), p.1342-1346

2005

Volltextzugriff (PDF)

Pulse oximetry in methemoglobinemia

American journal of diseases of children (1960), 1989-07, Vol.143 (7), p.845

1989

Volltextzugriff (PDF)

Familial acromelic frontonasal dysostosis: Autosomal dominant inheritance with reduced penetrance

American journal of medical genetics. Part A, 2004-08, Vol.128A (4), p.374-382

2004

Volltextzugriff (PDF)

A novel oculo-oto-facial dysplasia in a Native Alaskan community with autosomal recessive inheritance

American journal of medical genetics. Part A, 2006-04, Vol.140A (8), p.804-812

2006

Volltextzugriff (PDF)

Genetics of Progressive Hearing Loss

Seminars in hearing, 1995-08, Vol.16 (3), p.246-256

1995

Volltextzugriff (PDF)

Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and pro alpha 2 (I) collagen (COL1A2)

Human molecular genetics, 1992-05, Vol.1 (2), p.135-135

1992

Volltextzugriff (PDF)

Symbolic Shape Descriptors for Classifying Craniosynostosis Deformations from Skull Imaging

2005 IEEE Engineering in Medicine and Biology 27th Annual Conference, 2005, p.6325-6331

2005

Volltextzugriff (PDF)

Enhancing T cell therapy through TCR-signaling-responsive nanoparticle drug delivery

Nature biotechnology, 2018-09, Vol.36 (8), p.707-716

2018

Volltextzugriff (PDF)

Microtia: Epidemiology and genetics

American journal of medical genetics. Part A, 2012-01, Vol.158A (1), p.124-139

2012

Volltextzugriff (PDF)

Robin sequence: from diagnosis to development of an effective management plan

Pediatrics (Evanston), 2011-05, Vol.127 (5), p.936-948

2011

Volltextzugriff (PDF)

1 – 25 von 287

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(243)
Mit Volltextzugriff
(236)

Publikationsform

Sprache

Englisch
(284)
Französisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(197)
Life Sciences & Biomedicine
(157)
Humans
(142)
Biological And Medical Sciences
(81)
Male
(80)
Female
(76)
Medical Sciences
(65)
Animals
(43)
Genetics & Heredity
(40)
Adult
(39)
Middle Aged
(31)
Physical Sciences
(28)
Chemistry
(26)
Pharmacology. Drug Treatments
(25)
Pharmacology & Pharmacy
(23)
Fundamental And Applied Biological Sciences. Psychology
(22)
Risk Factors
(22)
Technology
(20)
Aged
(19)
Child
(18)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Syndromic craniosynostosis: from history to hydrogen bonds

Clinical care in craniofacial microsomia: A review of current management recommendations and opportunities to advance research

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

Mapping Human Telomere Regions with YAC and P1 Clones: Chromosome-Specific Markers for 27 Telomeres Including 149 STSs and 24 Polymorphisms for 14 Proterminal Regions

Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

VNTR and microsatellite polymorphisms within the subtelomeric region of 7q

GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease

Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and proα2 (1) collagen (COL1A2)

Linkage of preaxial polydactyly type 2 to 7q36

Aase syndrome: Novel radiographic features

New Scaphocephaly Severity Indices of Sagittal Craniosynostosis: A Comparative Study with Cranial Index Quantifications

A lethal syndrome resembling branchio-oculo facial syndrome

Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations

MDCT diagnosis of the child with posterior plagiocephaly

Pulse oximetry in methemoglobinemia

Familial acromelic frontonasal dysostosis: Autosomal dominant inheritance with reduced penetrance

A novel oculo-oto-facial dysplasia in a Native Alaskan community with autosomal recessive inheritance

Genetics of Progressive Hearing Loss

Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and pro alpha 2 (I) collagen (COL1A2)

Symbolic Shape Descriptors for Classifying Craniosynostosis Deformations from Skull Imaging

Enhancing T cell therapy through TCR-signaling-responsive nanoparticle drug delivery

Microtia: Epidemiology and genetics

Robin sequence: from diagnosis to development of an effective management plan

Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate

Suchergebnisse filtern