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...

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Journal of medical genetics, 2002-07, Vol.39 (7), p.478-483

2002

Volltextzugriff (PDF)

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

Nature genetics, 2000-08, Vol.25 (4), p.419-422

2000

Volltextzugriff (PDF)

Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene

Human genetics, 2001-06, Vol.108 (6), p.546-551

2001

Volltextzugriff (PDF)

Localization of the gene for Cowden disease to chromosome 10q22-23

Nature genetics, 1996-05, Vol.13 (1), p.114-116

1996

Volltextzugriff (PDF)

Germline PTEN mutations in Cowden syndrome-like families

Journal of medical genetics, 1998-11, Vol.35 (11), p.881-885

1998

Volltextzugriff (PDF)

Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (naxos disease) maps to 17q21

Circulation (New York, N.Y.), 1998-05, Vol.97 (20), p.2049-2058

1998

Volltextzugriff (PDF)

An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome

American journal of human genetics, 2003-05, Vol.72 (5), p.1261-1267

2003

Volltextzugriff (PDF)

Clinical and molecular features of the hereditary mixed polyposis syndrome

Gastroenterology (New York, N.Y. 1943), 1997-02, Vol.112 (2), p.327-334

1997

Volltextzugriff (PDF)

Localization of the gene for familial adenomatous polyposis on chromosome 5

Nature (London), 1987-08, Vol.328 (6131), p.614-616

1987

Volltextzugriff (PDF)

A Gene for Lymphedema-Distichiasis Maps to 16q24.3

American journal of human genetics, 1999-08, Vol.65 (2), p.427-432

1999

Volltextzugriff (PDF)

Lack of c-kit mutation in familial urticaria pigmentosa

British journal of dermatology (1951), 1999-05, Vol.140 (5), p.849-852

1999

Volltextzugriff (PDF)

Colonoscopy in asymptomatic individuals with a family history of colorectal cancer

Annals of surgical oncology, 2002-06, Vol.9 (5), p.439-443

2002

Volltextzugriff (PDF)

Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22

Human genetics, 2000-03, Vol.106 (3), p.351-354

2000

Volltextzugriff (PDF)

Genetic Predisposition to Cancer: The Consequences of a Delayed Diagnosis of Gorlin Syndrome

Clinical oncology (Royal College of Radiologists (Great Britain)), 2005-12, Vol.17 (8), p.650-654

2005

Volltextzugriff (PDF)

Pulmonary Masses Presenting 11 Years after Abdominal Surgery

Respiration, 2004-05, Vol.71 (3), p.295-297

2004

Volltextzugriff (PDF)

Frequency of familial colorectal cancer

British journal of surgery, 1991-10, Vol.78 (10), p.1162-1166

1991

Volltextzugriff (PDF)

Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome

The New England journal of medicine, 2008-12, Vol.359 (24), p.2567-2578

2008

Volltextzugriff (PDF)

Genetic mapping of the hereditary mixed polyposis syndrome to chromosome 6q

American journal of human genetics, 1996-04, Vol.58 (4), p.770-776

1996

Volltextzugriff (PDF)

Colonoscopy in symptomatic patients with positive family history of colorectal cancer

Anticancer research, 2000-05, Vol.20 (3B), p.1991

2000

Volltextzugriff (PDF)

Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb

Journal of medical genetics, 2000-09, Vol.37 (9), p.725-725

2000

Volltextzugriff (PDF)

Feasibility of family based screening for colorectal neoplasia: experience in one general surgical practice

Gut, 1993-01, Vol.34 (1), p.96-100

1993

Volltextzugriff (PDF)

Secondary hypertension and clinical genetics: usual presentation with unusual diagnosis

Journal of human hypertension, 1999, Vol.13 (1), p.79-80

1999

Volltextzugriff (PDF)

Muir-Torre syndrome: a variant of the cancer family syndrome

Journal of medical genetics, 1994-08, Vol.31 (8), p.627-631

1994

Volltextzugriff (PDF)

A new autosomal recessive syndrome of characteristic facies, joint contractures, skeletal abnormalities, and normal development: second report with further clinical delineation

Journal of medical genetics, 1995-10, Vol.32 (10), p.809-812

1995

Volltextzugriff (PDF)

1 – 25 von 138

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(125)
Mit Volltextzugriff
(121)

Publikationsform

Artikel
(137)
Berichte
(1)

Sprache

Englisch
(136)
Deutsch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome

Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene

Localization of the gene for Cowden disease to chromosome 10q22-23

Germline PTEN mutations in Cowden syndrome-like families

Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (naxos disease) maps to 17q21

An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome

Clinical and molecular features of the hereditary mixed polyposis syndrome

Localization of the gene for familial adenomatous polyposis on chromosome 5

A Gene for Lymphedema-Distichiasis Maps to 16q24.3

Lack of c-kit mutation in familial urticaria pigmentosa

Colonoscopy in asymptomatic individuals with a family history of colorectal cancer

Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22

Genetic Predisposition to Cancer: The Consequences of a Delayed Diagnosis of Gorlin Syndrome

Pulmonary Masses Presenting 11 Years after Abdominal Surgery

Frequency of familial colorectal cancer

Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome

Genetic mapping of the hereditary mixed polyposis syndrome to chromosome 6q

Colonoscopy in symptomatic patients with positive family history of colorectal cancer

Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb

Feasibility of family based screening for colorectal neoplasia: experience in one general surgical practice

Secondary hypertension and clinical genetics: usual presentation with unusual diagnosis

Muir-Torre syndrome: a variant of the cancer family syndrome

A new autosomal recessive syndrome of characteristic facies, joint contractures, skeletal abnormalities, and normal development: second report with further clinical delineation

Suchergebnisse filtern