SCOPUS 정보 검색 플랫폼

Volumn 56, Issue 1, 1980, Pages 59-62

Chromosomal studies of leukemic and preleukemic Fanconi's anemia patients - Examples of acquired 'chromosomal amplification'

(5) Berger, Roland a Bernheim, Alain a Le Coniat, Maryvonne a Vecchione, Danièle a Schaison, Gérard a

a SAINT LOUIS HOSPITAL (France)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD AND HEMOPOIETIC SYSTEM; CASE REPORT; CHROMOSOME 3Q; CHROMOSOME ABERRATION; CLONE; CYTOLOGY; DIAGNOSIS; ERYTHROLEUKEMIA; FANCONI ANEMIA; HEREDITY; HISTOLOGY; IN VITRO STUDY; PARTIAL TRISOMY 3; PRELEUKEMIA;

ADOLESCENT; ANEMIA, APLASTIC; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN; CHROMOSOMES, HUMAN, 1-3; CONSANGUINITY; FANCONI ANEMIA; FEMALE; FOLLOW-UP STUDIES; HUMANS; KARYOTYPING; LEUKEMIA, ERYTHROBLASTIC, ACUTE; MALE; PRELEUKEMIA;

EID: 0018973190 PISSN: 03406717 EISSN: 14321203 Source Type: Journal
DOI: 10.1007/BF00281569 Document Type: Article

Times cited : (28)

References (13)

1
- 0016677602
- Anomalies chromosomiques et anémie de Fanconi. Etude de 4 cas
- (1975) Nouv Rev Fr Hematol , vol.15 , pp. 539-550
- Berger, R.¹ Bussel, A.² Schenmetzler, C.³

2
- 0017736598
- Somatic segregation and Fanconi anemia
- (1977) Clin Genet , vol.11 , pp. 409-415
- Berger, R.¹ Bussel, A.² Schenmetzler, C.³

3
- 0017349665
- Fanconi anemia leading to acute myelomonocytic leukemia
- (1977) Cytogenetic studies Cancer , vol.39 , pp. 1163-1167
- Bourgeois, C.A.¹ Hill, F.G.H.²

4
- 0015260420
- Chromosome studies in Fanconi's anaemia before and after treatment with oxymetholone
- (1972) Pathology , vol.4 , pp. 27-33
- Crossen, P.E.¹ Mellor, J.E.L.² Ada, A.C.³ Gunz, F.W.⁴

5
- 84932438106
- Frocrain C, Tanzer J, Desmaret MC (1978) Preleukemic syndrome (“Belgian type”) in a patient with Fanconi's anemia. Symposium on Chromosomes et hémopathies, Poitiers

6
- 0014548063
- Chromosomal aberrations in two cases of inherited aplastic anemia with unusual clinical features
- (1969) Ann Intern Med , vol.71 , pp. 107-117
- Hirschman, R.J.¹ Shulman, N.R.² Abuelo, J.G.³ Whang-Peng, J.⁴

7
- 0016264916
- Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution
- (1974) Clin Genet , vol.5 , pp. 72-76
- Lisker, R.¹ Cobo de Gutierrez, A.²

8
- 84932429681
- Paris Conference. 1971 (1972) Standardization in Human Cytogenetics. Birth Defects: Orig Art Ser VIII: 7. The National Foundation, New York

9
- 84932483767
- Paris Conference, 1971; Supplement, 1975 (1975) Standardization in Human Cytogenetics. Birth Defects: Orig Art Ser XI:9. The National Foundation, New York

10
- 0017721977
- Fanconi's anaemia in adults: study of three families
- (1977) Haematologica (Pavia) , vol.62 , pp. 615-628
- Perona, G.¹ Cetto, G.L.² Bernadi, F.³ Todeschini, G.⁴ d'Andrea, F.⁵

11
- 0017623996
- Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemia
- (1977) Blut , vol.34 , pp. 119-132
- Schroeder, T.M.¹ Drings, P.² Beilner, P.³ Buchinger, G.⁴

12
- 0018619959
- Fanconi's anemia: terminal leukemia and “forme fruste” in one family
- (1979) Clin Genet , vol.16 , pp. 260-268
- Schroeder, T.M.¹ Pöhler, E.² Hufnagl, H.D.³ Stahl-Mauge, C.⁴

13
- 0015700968
- Nonrandom distribution of chromosome breaks in Fanconi's anaemia
- (1973) Cytogenet Cell Genet , vol.12 , pp. 423-434
- Von Koskull, H.¹ Aula, P.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.