UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 25

Sortiert nach

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

Cell, 1993-07, Vol.74 (1), p.127-134

1993

Volltextzugriff (PDF)

P1-54 Maternal and child glutathione-S-transferase M1 and T1 polymorphisms modify effect of maternal smoking in pregnancy on childhood lung function

Early human development, 2007, Vol.83, p.S97-S97

2007

Volltextzugriff (PDF)

3A-7 Maternal and child glutathione-S-transferase M1 polymorphism modifies risk of childhood asthma associated with prenatal paracetamol exposure

Early human development, 2007, Vol.83, p.S59-S60

2007

Volltextzugriff (PDF)

Radiological malformations of the ear in pendred syndrome

Clinical radiology, 1998-04, Vol.53 (4), p.268-273

1998

Volltextzugriff (PDF)

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

The Lancet (British edition), 1992-12, Vol.340 (8832), p.1376-1379

1992

Volltextzugriff (PDF)

Uniparental paternal disomy in Angelman's syndrome

The Lancet (British edition), 1991-03, Vol.337 (8743), p.694-697

1991

Volltextzugriff (PDF)

RISK ESTIMATION AND SCREENING IN FAMILIES OF PATIENTS WITH MEDULLARY THYROID CARCINOMA

The Lancet (British edition), 1988-02, Vol.331 (8582), p.397-401

1988

Volltextzugriff (PDF)

Multiple origins for phenylketonuria in Europe

American journal of human genetics, 1992-12, Vol.51 (6), p.1355-1365

1992

Volltextzugriff (PDF)

A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.885-894

1991

Volltextzugriff (PDF)

A CLINICALLY USEFUL DNA PROBE CLOSELY LINKED TO HAEMOPHILIA A

The Lancet (British edition), 1984-07, Vol.324 (8393), p.6-8

1984

Volltextzugriff (PDF)

USE OF X CHROMOSOME INACTIVATION ANALYSIS TO ESTABLISH CARRIER STATUS FOR X-LINKED SEVERE COMBINED IMMUNODEFICIENCY

The Lancet (British edition), 1988-04, Vol.331 (8588), p.729-732

1988

Volltextzugriff (PDF)

Multicentre study of antenatal calyceal dilatation detected by ultrasound

The Lancet (British edition), 1990-10, Vol.336 (8719), p.875-875

1990

Volltextzugriff (PDF)

Acquired increases of fetal haemoglobin in adults

Pembrey, M.E

1978

Volltextzugriff (PDF)

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis

American journal of medical genetics, 1994-06, Vol.51 (2), p.176-184

1994

Volltextzugriff (PDF)

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome

Human genetics, 1985-01, Vol.70 (3), p.249-255

1985

Volltextzugriff (PDF)

Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males

Human genetics, 1986-09, Vol.74 (1), p.93-97

1986

Volltextzugriff (PDF)

Unusual presentation of fragile X syndrome

The Lancet (British edition), 1990-11, Vol.336 (8723), p.1131-1131

1990

Volltextzugriff (PDF)

The major cystic fibrosis mutation in a British population

Human genetics, 1990-12, Vol.86 (2), p.236-237

1990

Volltextzugriff (PDF)

FETAL LIVER BIOPSY FOR PRENATAL DIAGNOSIS OF ORNITHINE CARBAMYL TRANSFERASE DEFICIENCY

The Lancet (British edition), 1982-08, Vol.320 (8293), p.297-300

1982

Volltextzugriff (PDF)

MATERNAL SYNTHESIS OF HÆMOGLOBIN F IN PREGNANCY

The Lancet (British edition), 1973-06, Vol.301 (7816), p.1350-1355

1973

Volltextzugriff (PDF)

α1-ANTITRYPSIN PHENOTYPES IN RHEUMATOID ARTHRITIS AND ANKYLOSING SPONDYLITIS

The Lancet (British edition), 1977-12, Vol.310 (8052), p.1358-1359

1977

Volltextzugriff (PDF)

Neuropathologic changes in ornithine carbamoyl transferase deficiency

The Journal of pediatrics, 1986-12, Vol.109 (6), p.1074-1074

1986

Volltextzugriff (PDF)

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

Human genetics, 1985-01, Vol.71 (2), p.182-183

1985

Volltextzugriff (PDF)

FAMILIAL SIDEROBLASTIC ANÆMIA: PROBLEM OF Xg AND X CHROMOSOME INACTIVATION

The Lancet (British edition), 1970-10, Vol.296 (7676), p.744-748

1970

Volltextzugriff (PDF)

NORMAL CHILD AFTER MATERNAL THALIDOMIDE INGESTION IN CRITICAL PERIOD OF PREGNANCY

The Lancet (British edition), 1970-02, Vol.295 (7641), p.275-277

1970

Volltextzugriff (PDF)

1 – 25 von 25

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(24)

Publikationsform

Artikel
(24)
Dissertationen
(1)

Sprache

Englisch
(25)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

P1-54 Maternal and child glutathione-S-transferase M1 and T1 polymorphisms modify effect of maternal smoking in pregnancy on childhood lung function

3A-7 Maternal and child glutathione-S-transferase M1 polymorphism modifies risk of childhood asthma associated with prenatal paracetamol exposure

Radiological malformations of the ear in pendred syndrome

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

Uniparental paternal disomy in Angelman's syndrome

RISK ESTIMATION AND SCREENING IN FAMILIES OF PATIENTS WITH MEDULLARY THYROID CARCINOMA

Multiple origins for phenylketonuria in Europe

A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity

A CLINICALLY USEFUL DNA PROBE CLOSELY LINKED TO HAEMOPHILIA A

USE OF X CHROMOSOME INACTIVATION ANALYSIS TO ESTABLISH CARRIER STATUS FOR X-LINKED SEVERE COMBINED IMMUNODEFICIENCY

Multicentre study of antenatal calyceal dilatation detected by ultrasound

Acquired increases of fetal haemoglobin in adults

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome

Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males

Unusual presentation of fragile X syndrome

The major cystic fibrosis mutation in a British population

FETAL LIVER BIOPSY FOR PRENATAL DIAGNOSIS OF ORNITHINE CARBAMYL TRANSFERASE DEFICIENCY

MATERNAL SYNTHESIS OF HÆMOGLOBIN F IN PREGNANCY

α1-ANTITRYPSIN PHENOTYPES IN RHEUMATOID ARTHRITIS AND ANKYLOSING SPONDYLITIS

Neuropathologic changes in ornithine carbamoyl transferase deficiency

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

FAMILIAL SIDEROBLASTIC ANÆMIA: PROBLEM OF Xg AND X CHROMOSOME INACTIVATION

NORMAL CHILD AFTER MATERNAL THALIDOMIDE INGESTION IN CRITICAL PERIOD OF PREGNANCY

Suchergebnisse filtern