Arwert F - Search Results

1

Early prenatal diagnosis of Fanconi anaemia in a twin pregnancy, using DNA analysis.

Kwee ML, Lo Ten Foe JR, Arwert F, Pals G, Madan K, Nieuwint A, In't Veld PA, Van der Horst AR, Van Vugt JM, Ten Kate LP. Kwee ML, et al. Among authors: arwert f. Prenat Diagn. 1996 Apr;16(4):345-8. doi: 10.1002/(SICI)1097-0223(199604)16:4<345::AID-PD852>3.0.CO;2-9. Prenat Diagn. 1996. PMID: 8734810

2

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.

Joenje H, Lo ten Foe JR, Oostra AB, van Berkel CG, Rooimans MA, Schroeder-Kurth T, Wegner RD, Gille JJ, Buchwald M, Arwert F. Joenje H, et al. Among authors: arwert f. Blood. 1995 Sep 15;86(6):2156-60. Blood. 1995. PMID: 7662964 Free article.

3

Complementation testing and genetic classification of Fanconi's anaemia.

Joenje H, Lo Ten Foe JR, Arwert F, ten Kate LP. Joenje H, et al. Among authors: arwert f. Lancet. 1994 Apr 2;343(8901):862. doi: 10.1016/s0140-6736(94)92069-9. Lancet. 1994. PMID: 7908113 No abstract available.

4

Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia C gene, FAC.

Lo Ten Foe JR, Rooimans MA, Joenje H, Arwert F. Lo Ten Foe JR, et al. Among authors: arwert f. Hum Mutat. 1996;7(3):264-5. doi: 10.1002/(SICI)1098-1004(1996)7:3<264::AID-HUMU11>3.0.CO;2-0. Hum Mutat. 1996. PMID: 8829660 No abstract available.

5

Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant.

Lo ten Foe JR, Barel MT, Thuss P, Digweed M, Arwert F, Joenje H. Lo ten Foe JR, et al. Among authors: arwert f. Hum Genet. 1996 Nov;98(5):522-3. doi: 10.1007/s004390050252. Hum Genet. 1996. PMID: 8882868

6

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

Lo Ten Foe JR, Rooimans MA, Bosnoyan-Collins L, Alon N, Wijker M, Parker L, Lightfoot J, Carreau M, Callen DF, Savoia A, Cheng NC, van Berkel CG, Strunk MH, Gille JJ, Pals G, Kruyt FA, Pronk JC, Arwert F, Buchwald M, Joenje H. Lo Ten Foe JR, et al. Among authors: arwert f. Nat Genet. 1996 Nov;14(3):320-3. doi: 10.1038/ng1196-320. Nat Genet. 1996. PMID: 8896563

7

An atypical case of Fanconi anemia in elderly sibs.

Kwee ML, van der Kleij JM, van Essen AJ, Begeer JH, Joenje H, Arwert F, ten Kate LP. Kwee ML, et al. Among authors: arwert f. Am J Med Genet. 1997 Jan 31;68(3):362-6. Am J Med Genet. 1997. PMID: 9024573

8

Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.

Lo Ten Foe JR, Kwee ML, Rooimans MA, Oostra AB, Veerman AJ, van Weel M, Pauli RM, Shahidi NT, Dokal I, Roberts I, Altay C, Gluckman E, Gibson RA, Mathew CG, Arwert F, Joenje H. Lo Ten Foe JR, et al. Among authors: arwert f. Eur J Hum Genet. 1997 May-Jun;5(3):137-48. Eur J Hum Genet. 1997. PMID: 9272737

9

Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstream.

Lo Ten Foe JR, Kruyt FA, Zweekhorst MB, Pals G, Gibson RA, Mathew CG, Joenje H, Arwert F. Lo Ten Foe JR, et al. Among authors: arwert f. Hum Mutat. 1998;Suppl 1:S25-7. doi: 10.1002/humu.1380110109. Hum Mutat. 1998. PMID: 9452030 No abstract available.

10

Confounding factors in the diagnosis of Fanconi anaemia.

Joenje H, Arwert F, Kwee ML, Madan K, Hoehn H. Joenje H, et al. Among authors: arwert f. Am J Med Genet. 1998 Oct 12;79(5):403-5. doi: 10.1002/(sici)1096-8628(19981012)79:5<403::aid-ajmg16>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9779812 No abstract available.

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