161 related articles for article (PubMed ID: 5771220)
1. Clinical and chromosome studies in Fanconi's aplastic anaemia.
Perkins J; Timson J; Emery AE
J Med Genet; 1969 Mar; 6(1):28-33. PubMed ID: 5771220
[No Abstract] [Full Text] [Related]
2. [Spontaneous chromosomal instability in the rare hereditary diseases: Fanconi's anemia and Bloom's syndrome].
Schroeder TM
Dtsch Med Wochenschr; 1973 Nov; 98(46):2213-5. PubMed ID: 4757391
[No Abstract] [Full Text] [Related]
3. Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution.
Lisker R; Cobo de Gutiérrez A
Clin Genet; 1974 Jan; 5(1):72-6. PubMed ID: 4839030
[No Abstract] [Full Text] [Related]
4. [Chromosomal study of Fanconi's aplastic anemia. Apropos of 2 cases].
Ortega Aramburu JJ; García-San Miguel J
Sangre (Barc); 1972; 17(1):87-100. PubMed ID: 5016799
[No Abstract] [Full Text] [Related]
5. Fanconi's anaemia in adults: study of three families.
Perona G; Cetto GL; Bernardi F; Todeschini G; D'Andrea F
Haematologica; 1977 Dec; 62(6):615-28. PubMed ID: 414973
[No Abstract] [Full Text] [Related]
6. Fanconi's anemia: clues to early recognition.
Pochedly C
Clin Pediatr (Phila); 1972 Jan; 11(1):20-4. PubMed ID: 5061325
[No Abstract] [Full Text] [Related]
7. Fanconi's anaemia.
Beard ME; Young DE; Bateman CJ; McCarthy GT; Smith ME; Sinclair L; Franklin AW; Scott RB
Q J Med; 1973 Apr; 42(166):403-22. PubMed ID: 4362013
[No Abstract] [Full Text] [Related]
8. Dominantly transmitted hematologic dysfunction clinically similar to Fanconi's anemia.
Alter CL; Levine PH; Bennett J; Kessler C; Rick M; Washburn RG; Gallin JI; Miller RW; Auerbach AD
Am J Hematol; 1989 Dec; 32(4):241-7. PubMed ID: 2816920
[TBL] [Abstract][Full Text] [Related]
9. Fanconi's anaemia; chromosome breakage in a large African family.
Meme JS; Greipenberg U; Kähkönen M
Hereditas; 1980; 93(2):255-60. PubMed ID: 7440242
[No Abstract] [Full Text] [Related]
10. [Chromosome aberrations in Fanconi's aplastic anemia].
Prandota J; Haus O
Pediatr Pol; 1985 Jan; 60(1):87-9. PubMed ID: 4034293
[No Abstract] [Full Text] [Related]
11. Fanconi's aplastic anemia, analysis of 18 cases.
Gözdaşoğlu S; Cavdar AO; Arcasoy A; Babacan E; Sanal O
Acta Haematol; 1980; 64(3):131-5. PubMed ID: 6778045
[TBL] [Abstract][Full Text] [Related]
12. [A case of Fanconi's anemia. Clinical, hematological and cytogenetic study].
Puşkas G; Rusnac C; Csidey J; Puşcaş E
Pediatria (Bucur); 1968; 17(1):33-40. PubMed ID: 4386359
[No Abstract] [Full Text] [Related]
13. Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement.
Schroeder TM; German J
Humangenetik; 1974; 25(4):299-306. PubMed ID: 4464237
[No Abstract] [Full Text] [Related]
14. [Fanconi's hypoplastic anemia].
Prandota J; Pellar J; Nienartowicz B; Noczynska A
Padiatr Grenzgeb; 1987; 26(4):247-54. PubMed ID: 3658473
[No Abstract] [Full Text] [Related]
15. Constitutional aplastic anaemia with congenital anomalies (Fanconi's anaemia)--a family study.
Da Costa JL; Jayaratnam FJ; Seah CS
J Singapore Paediatr Soc; 1969 Apr; 11(1):73-81. PubMed ID: 5366342
[No Abstract] [Full Text] [Related]
16. Distribution of chromosome breaks in measles, Fanconi's anemia and controls.
von Koskull H; Aula P
Hereditas; 1977; 87(1):1-10. PubMed ID: 591354
[No Abstract] [Full Text] [Related]
17. Cytogenetical and clinical investigations in aplastic anaemia (Fancomi's type).
Guanti G; Petrinelli P; Schettini F
Humangenetik; 1971; 13(3):222-33. PubMed ID: 5114677
[No Abstract] [Full Text] [Related]
18. Inherited aplastic anaemia with increased endoreduplications: a new syndrome of Fanconi's anaemia variant?
Dosik H; Steier W; Lubiniecki A
Br J Haematol; 1979 Jan; 41(1):77-82. PubMed ID: 217401
[TBL] [Abstract][Full Text] [Related]
19. [Chromosome changes in Fanconi's anemia (FA) and clinical course of the disease (familial constitutional panmyelopathy)].
Traczyk Z; Rostkowska J; Kolakowski L
Pol Tyg Lek; 1972 Nov; 27(45):1758-61. PubMed ID: 4636501
[No Abstract] [Full Text] [Related]
20. Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.
Shahid MJ; Khouri FP; Ballas SK
J Med Genet; 1972 Dec; 9(4):474-8. PubMed ID: 4646560
[No Abstract] [Full Text] [Related]
[Next] [New Search]
