C G van Berkel
Overview
Explore the profile of C G van Berkel including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
614
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Recent Articles
1.
Leegwater P, Vermeulen G, Konst A, Naidu S, Mulders J, Visser A, et al.
Nat Genet
. 2001 Nov;
29(4):383-8.
PMID: 11704758
Leukoencephalopathy with vanishing white matter (VWM) is an inherited brain disease that occurs mainly in children. The course is chronic-progressive with additional episodes of rapid deterioration following febrile infection or...
2.
de Winter J, Leveille F, van Berkel C, Rooimans M, van der Weel L, Steltenpool J, et al.
Am J Hum Genet
. 2000 Sep;
67(5):1306-8.
PMID: 11001585
Fanconi anemia (FA) is an autosomal recessive chromosomal instability syndrome with at least seven different complementation groups. Four FA genes (FANCA, FANCC, FANCF, and FANCG) have been identified, and two...
3.
Joenje H, Levitus M, Waisfisz Q, DAndrea A, Garcia-Higuera I, Pearson T, et al.
Am J Hum Genet
. 2000 Aug;
67(3):759-62.
PMID: 10936108
Fanconi anemia (FA) is an autosomal recessive disorder with diverse clinical symptoms and extensive genetic heterogeneity. Of eight FA genes that have been implicated on the basis of complementation studies,...
4.
de Winter J, Rooimans M, van der Weel L, van Berkel C, Alon N, de Groot J, et al.
Nat Genet
. 1999 Dec;
24(1):15-6.
PMID: 10615118
No abstract available.
5.
Waisfisz Q, Morgan N, Savino M, de Winter J, van Berkel C, Hoatlin M, et al.
Nat Genet
. 1999 Aug;
22(4):379-83.
PMID: 10431244
Somatic mosaicism due to reversion of a pathogenic allele to wild type has been described in several autosomal recessive disorders. The best known mechanism involves intragenic mitotic recombination or gene...
6.
Cleton-Jansen A, Moerland E, Pronk J, van Berkel C, Apostolou S, Crawford J, et al.
Br J Cancer
. 1999 Mar;
79(7-8):1049-52.
PMID: 10098735
The recently identified Fanconi anaemia A (FAA) gene is located on chromosomal band 16q24.3 within a region that has been frequently reported to show loss of heterozygosity (LOH) in breast...
7.
Wijker M, Morgan N, Herterich S, van Berkel C, Tipping A, Gross H, et al.
Eur J Hum Genet
. 1999 Mar;
7(1):52-9.
PMID: 10094191
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chromosomal fragility, bone-marrow failure, congenital abnormalities and cancer. The gene for complementation group A (FAA), which accounts for...
8.
de Winter J, Waisfisz Q, Rooimans M, van Berkel C, Alon N, Carreau M, et al.
Nat Genet
. 1998 Nov;
20(3):281-3.
PMID: 9806548
Fanconi anemia (FA) is an autosomal recessive disease with diverse clinical symptoms including developmental anomalies, bone marrow failure and early occurrence of malignancies. In addition to spontaneous chromosome instability, FA...
9.
Joenje H, Oostra A, Wijker M, di Summa F, van Berkel C, Rooimans M, et al.
Am J Hum Genet
. 1997 Oct;
61(4):940-4.
PMID: 9382107
Fanconi anemia (FA) is an autosomal recessive chromosomal breakage disorder with diverse clinical symptoms including progressive bone marrow failure and increased cancer risk. FA cells are hypersensitive to crosslinking agents,...
10.
Foe J, Rooimans M, Alon N, Wijker M, Parker L, Lightfoot J, et al.
Nat Genet
. 1996 Dec;
14(4):488.
PMID: 8944034
No abstract available.