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...

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Human mutation, 1998, Vol.11 (5), p.387-394

1998

Volltextzugriff (PDF)

A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment

Journal of medical genetics, 2000-09, Vol.37 (9), p.692-694

2000

Volltextzugriff (PDF)

A gene for ataxic cerebral palsy maps to chromosome 9p12-q12

European journal of human genetics : EJHG, 2000-04, Vol.8 (4), p.267-272

2000

Volltextzugriff (PDF)

Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primers

Nucleic acids research, 1996-06, Vol.24 (11), p.2190-2191

1996

Volltextzugriff (PDF)

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31

European journal of human genetics : EJHG, 2000-12, Vol.8 (12), p.991-993

2000

Volltextzugriff (PDF)

The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2

European journal of human genetics : EJHG, 1999-10, Vol.7 (7), p.815-820

1999

Volltextzugriff (PDF)

Population genomics and dental public health

Community dental health, 2006-09, Vol.23 (3), p.130

2006

Volltextzugriff (PDF)

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)

Human mutation, 1995, Vol.5 (3), p.251-259

1995

Volltextzugriff (PDF)

SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1)

Human molecular genetics, 1994-05, Vol.3 (5), p.827-828

1994

Volltextzugriff (PDF)

Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.56-58

2001

Volltextzugriff (PDF)

Genetics – getting personal

Drug discovery today, 2008-03, Vol.13 (5), p.189-191

Lench, Nicholas J.

2008

Volltextzugriff (PDF)

A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3

Mammalian genome, 1995-10, Vol.6 (10), p.725-731

1995

Volltextzugriff (PDF)

YAC clones that extend the human chromosome 12cen-12q15 region contig map

Mammalian genome, 1996-10, Vol.7 (10), p.780-783

1996

Volltextzugriff (PDF)

Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafin

Archives of oral biology, 1996-05, Vol.41 (5), p.445-452

1996

Volltextzugriff (PDF)

DNA Marker D11S384 Shows Zero Recombination with the Ataxia-telangiectasia Locus in North American Families

International journal of radiation biology, 1994, Vol.66 (6), p.S67-S69

1994

Volltextzugriff (PDF)

Genetic aspects of ataxia telangiectasia

Advances in neurology, 1993, Vol.61, p.115

1993

Volltextzugriff (PDF)

An anonymous DNA probe (NL32) recognises a MspI polymorphism on human chromosome 1 [D1S84]

Nucleic acids research, 1988-12, Vol.16 (24), p.11854-11854

1988

Volltextzugriff (PDF)

Mapping of the DFNB1 locus

Advances in oto-rhino-laryngology, 2000, Vol.56, p.116-123

2000

Volltextzugriff (PDF)

cDNA Cloning, Genomic Organization, and Chromosomal Localization of a Novel Human Gene That Encodes a Kinesin-Related Protein Highly Similar to Mouse Kif3C

Biochemical and biophysical research communications, 1998-01, Vol.242 (2), p.407-412

1998

Volltextzugriff (PDF)

Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts

European journal of cancer. Part B, Oral oncology, 1996-05, Vol.32 (3), p.202-206

1996

Volltextzugriff (PDF)

Isolation and characterisation of a cDNA encoding the precursor for a novel member of the Acyl-CoA dehydrogenase gene family

Biochimica et biophysica acta, 1999-09, Vol.1446 (3), p.371-376

1999

Volltextzugriff (PDF)

Inflammatory bowel disease is linked to 19p13 and associated with ICAM‐1

Inflammatory bowel diseases, 2004-05, Vol.10 (3), p.173-181

2004

Volltextzugriff (PDF)

PP2.0 – 2107 A new approach to genetic diagnosis in early infantile epileptic encephalopathy and severe neurodevelopmental delay using a gene panel

European journal of paediatric neurology, 2013-09, Vol.17, p.S33-S33

2013

Volltextzugriff (PDF)

Immunoglobulin gene rearrangements in lymphoplasmacytic infiltrates of labial salivary glands in Sjögren's syndrome. A possible predictor of lymphoma development

Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 1995-06, Vol.79 (6), p.723-729

1995

Volltextzugriff (PDF)

Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans

Molecular genetics and metabolism, 2002-09, Vol.77 (1), p.68-79

2002

Volltextzugriff (PDF)

1 – 25 von 57

Suche als RSS-Feed

Aktive Filter

ThemaBiological And Medical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(45)

Publikationsform

Sprache

Englisch
(57)
Japanisch
(8)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment

A gene for ataxic cerebral palsy maps to chromosome 9p12-q12

Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primers

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31

The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2

Population genomics and dental public health

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)

SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1)

Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation

Genetics – getting personal

A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3

YAC clones that extend the human chromosome 12cen-12q15 region contig map

Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafin

DNA Marker D11S384 Shows Zero Recombination with the Ataxia-telangiectasia Locus in North American Families

Genetic aspects of ataxia telangiectasia

An anonymous DNA probe (NL32) recognises a MspI polymorphism on human chromosome 1 [D1S84]

Mapping of the DFNB1 locus

cDNA Cloning, Genomic Organization, and Chromosomal Localization of a Novel Human Gene That Encodes a Kinesin-Related Protein Highly Similar to Mouse Kif3C

Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts

Isolation and characterisation of a cDNA encoding the precursor for a novel member of the Acyl-CoA dehydrogenase gene family

Inflammatory bowel disease is linked to 19p13 and associated with ICAM‐1

PP2.0 – 2107 A new approach to genetic diagnosis in early infantile epileptic encephalopathy and severe neurodevelopmental delay using a gene panel

Immunoglobulin gene rearrangements in lymphoplasmacytic infiltrates of labial salivary glands in Sjögren's syndrome. A possible predictor of lymphoma development

Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans

Aktive Filter

Suchergebnisse filtern