Normal view MARC view ISBD view

New clinical syndromes under regular intermittent hemodialysis. [electronic resource]

By:

Loew, H

Contributor(s):

Producer: 19760430Description: 239-76 p. digitalISSN:

0070-2188

Subject(s): Online resources:

Available from publisher's website

In: Current topics in pathology. Ergebnisse der Pathologie vol. 61

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article; Review

There are no comments on this title.

to post a comment.

Back to results

1 First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
by McKay, Victoria
2 Identifying Lynch Syndrome in Women Presenting With Endometrial Carcinoma Under the Age of 50 Years.
by Anagnostopoulos, Antonios
3 Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease.
by Weedon, Michael N
4 Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.
by Kalidas, Kamini
5 Constitutional trisomy 8 and Behçet syndrome.
by Becker, Kristin
6 Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.
by Klopocki, Eva
7 EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome.
by Pathak, Sagar J
8 Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations.
by Bancroft, Elizabeth K
9 TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism.
by Harley, Margaret E
10 Gene-gene interactions in breast cancer susceptibility.
by Turnbull, Clare
11 Germline mutations in RAD51D confer susceptibility to ovarian cancer.
by Loveday, Chey
12 Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes
by Andrews, Katrina A
13 Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.
by Whitworth, James
14 Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.
by Ruark, Elise
15 Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
by Beunders, Gea
16 Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study.
by Bancroft, Elizabeth K
17 Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
by Mikropoulos, Christos
18 Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
by Mikropoulos, Christos
19 Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.
by Page, Elizabeth C