214 related articles for article (PubMed ID: 7545870)
1. Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome.
Chrzanowska KH; Kleijer WJ; Krajewska-Walasek M; Białecka M; Gutkowska A; Goryluk-Kozakiewicz B; Michałkiewicz J; Stachowski J; Gregorek H; Lysón-Wojciechowska G
Am J Med Genet; 1995 Jul; 57(3):462-71. PubMed ID: 7545870
[TBL] [Abstract][Full Text] [Related]
2. [Microcephaly with chromosomal instability and immunodeficiency--Nijmegen syndrome].
Chrzanowska KH
Pediatr Pol; 1996 Mar; 71(3):223-34. PubMed ID: 8966094
[TBL] [Abstract][Full Text] [Related]
3. Nijmegen Breakage syndrome: a progress report.
Weemaes CM; Smeets DF; van der Burgt CJ
Int J Radiat Biol; 1994 Dec; 66(6 Suppl):S185-8. PubMed ID: 7836846
[TBL] [Abstract][Full Text] [Related]
4. Variants of Nijmegen breakage syndrome and ataxia telangiectasia.
Weemaes CM; Smeets DF; Horstink M; Haraldsson A; Bakkeren JA
Immunodeficiency; 1993; 4(1-4):109-11. PubMed ID: 7513225
[TBL] [Abstract][Full Text] [Related]
5. Further delineation of the Nijmegen breakage syndrome.
Taalman RD; Hustinx TW; Weemaes CM; Seemanová E; Schmidt A; Passarge E; Scheres JM
Am J Med Genet; 1989 Mar; 32(3):425-31. PubMed ID: 2786340
[TBL] [Abstract][Full Text] [Related]
6. A new chromosomal instability disorder confirmed by complementation studies.
Wegner RD; Metzger M; Hanefeld F; Jaspers NG; Baan C; Magdorf K; Kunze J; Sperling K
Clin Genet; 1988 Jan; 33(1):20-32. PubMed ID: 3277755
[TBL] [Abstract][Full Text] [Related]
7. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E
Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202
[TBL] [Abstract][Full Text] [Related]
8. Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child.
Barbi G; Scheres JM; Schindler D; Taalman RD; Rodens K; Mehnert K; Müller M; Seyschab H
Am J Med Genet; 1991 Jul; 40(1):44-50. PubMed ID: 1887849
[TBL] [Abstract][Full Text] [Related]
9. Chromosomal breakage syndromes.
Carney JP
Curr Opin Immunol; 1999 Aug; 11(4):443-7. PubMed ID: 10448147
[TBL] [Abstract][Full Text] [Related]
10. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.
Digweed M; Sperling K
DNA Repair (Amst); 2004; 3(8-9):1207-17. PubMed ID: 15279809
[TBL] [Abstract][Full Text] [Related]
11. Possible new variant of Nijmegen breakage syndrome.
Der Kaloustian VM; Kleijer W; Booth A; Auerbach AD; Mazer B; Elliott AM; Abish S; Usher R; Watters G; Vekemans M; Eydoux P
Am J Med Genet; 1996 Oct; 65(1):21-6. PubMed ID: 8914736
[TBL] [Abstract][Full Text] [Related]
12. Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndrome.
Di Rocco M; Arslanian A; Romanengo M; Dagna-Bricarelli F; Borrone C
J Med Genet; 1999 Feb; 36(2):159-60. PubMed ID: 10051019
[TBL] [Abstract][Full Text] [Related]
13. [Ring chromosome 17 and recurring pneumopathy].
Lambruschini Ferri N; Ortola Castells ME; Rosell Andreo J; Ballesta Martínez F
An Esp Pediatr; 1989 Nov; 31(5):478-80. PubMed ID: 2694873
[No Abstract] [Full Text] [Related]
14. Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome.
Sullivan KE; Veksler E; Lederman H; Lees-Miller SP
Clin Immunol Immunopathol; 1997 Jan; 82(1):43-8. PubMed ID: 9000041
[TBL] [Abstract][Full Text] [Related]
15. Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome.
Green AJ; Yates JR; Taylor AM; Biggs P; McGuire GM; McConville CM; Billing CJ; Barnes ND
Arch Dis Child; 1995 Nov; 73(5):431-4. PubMed ID: 8554361
[TBL] [Abstract][Full Text] [Related]
16. Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder.
Seemanová E; Passarge E; Beneskova D; Houstĕk J; Kasal P; Sevcíková M
Am J Med Genet; 1985 Apr; 20(4):639-48. PubMed ID: 3857858
[TBL] [Abstract][Full Text] [Related]
17. Positional cloning of the gene for Nijmegen breakage syndrome.
Matsuura S; Tauchi H; Nakamura A; Kondo N; Sakamoto S; Endo S; Smeets D; Solder B; Belohradsky BH; Der Kaloustian VM; Oshimura M; Isomura M; Nakamura Y; Komatsu K
Nat Genet; 1998 Jun; 19(2):179-81. PubMed ID: 9620777
[TBL] [Abstract][Full Text] [Related]
18. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
Kotzot D; Richter K; Gierth-Fiebig K
Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
[TBL] [Abstract][Full Text] [Related]
19. [Immunodeficiency and chromosome instability].
Weemaes CM; Bakkeren JA; Hustinx TW; van Munster PJ; Scheres JM
Tijdschr Kindergeneeskd; 1988 Oct; 56(5):209-12. PubMed ID: 3206518
[TBL] [Abstract][Full Text] [Related]
20. [Clinico-genetic diagnosis of ataxia telangiectatica (Louis-Bar syndrome)].
Fuhrmann E; Pfeiffer L; Zschenderlein R; Leonhardt T; Melster U; Kölmel HW
Nervenarzt; 1993 Feb; 64(2):140-2. PubMed ID: 8450897
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
