Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Showing 1 to 12 of 589 entries
Sorted by: Best Match Show Resources per page
Chronic granulocytic leukemia occurring in blast crisis.

Archives of pathology & laboratory medicine

Kapadia SB, Krause JR, Pan SF, Cotelingam J, Nitiyanant P.
PMID: 287416
Arch Pathol Lab Med. 1979 Jun;103(6):291-2.

Cytogenetic studies of marrow using chromosomal banding techniques revealed the presence of the Philadelphia (PH1) chromosome in two patients with clinical and hematologic findings of acute myelogenous leukemia (AML). A review of the literature since the use of chromosomal...

c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders.

Proceedings of the National Academy of Sciences of the United States of America

Le Beau MM, Westbrook CA, Diaz MO, Rowley JD.
PMID: 2413444
Proc Natl Acad Sci U S A. 1985 Oct;82(19):6692-6. doi: 10.1073/pnas.82.19.6692.
Free PMC Article

The proto-oncogene c-src has been mapped to two bands in human chromosomes, 1p36 and 20q13, both of which are involved in rearrangements in human tumors. In particular, deletions (loss of part of a chromosome) of the long arm of...

Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions.


Kakati S, Hayata I, Oshimura M, Sandberg AA.
PMID: 1192362
Cancer. 1975 Nov;36(5):1729-38. doi: 10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>;2-#.

Cells from five cancer effusions (two ovarian carcinomas, two lung cancers, and one carcinoma of the breast) were analyzed by G-, C-, and Q-banding techniques. The following observations were made: 1) The origin of some marker chromosomes could be...

Follow-up of infants with amniotic fluid trisomy 20 mosaicism.

American journal of medical genetics

Abuelo DN, Barsel-Bowers G, Zartler AS.
PMID: 3728566
Am J Med Genet. 1986 Jul;24(3):475-81. doi: 10.1002/ajmg.1320240310.

The finding of trisomy 20 mosaicism in amniotic fluid is a cause of considerable anxiety for both physicians and parents. Although the significance of this finding is still not clear, some reassurance can be given to prospective parents, since...

Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus.


Kim MA.
PMID: 4837300
Humangenetik. 1974 Mar 28;21(4):331-40. doi: 10.1007/BF00273371.

No abstract available.

Isolation of duplicated human c-src genes located on chromosomes 1 and 20.

Molecular and cellular biology

Parker RC, Mardon G, Lebo RV, Varmus HE, Bishop JM.
PMID: 2581127
Mol Cell Biol. 1985 Apr;5(4):831-8. doi: 10.1128/mcb.5.4.831-838.1985.
Free PMC Article

The oncogene (v-src) of Rous sarcoma virus apparently arose by transduction of the chicken gene known as c-src(chicken). We isolated DNA fragments representative of two src-related loci from recombinant DNA bacteriophage libraries of the human genome. One of these...

Chromosome studies in untreated polycythaemia vera.

Scandinavian journal of haematology

Westin J, Wahlström J, Swolin B.
PMID: 968448
Scand J Haematol. 1976 Sep;17(3):183-96. doi: 10.1111/j.1600-0609.1976.tb01174.x.

Bone marrow chromosomes were studied in a series of 50 consecutive, unselected cases of untreated polycythaemia vera (PV). A pathological cell line was present in 7 patients (= 14%). 3 patients each had 1 extra chromosome no. 8 and...

Trisomy of the short arm of chromosome 10.

Journal of medical genetics

Nakagome Y, Kobayashi H.
PMID: 1219122
J Med Genet. 1975 Dec;12(4):412-4. doi: 10.1136/jmg.12.4.412.
Free PMC Article

A case of a fetus with multiple malformations is described. The mother showed a 46,XX,rcp(10;22) (p11;p11) karyotype. Amniocentesis at the 16th week of gestation revealed that the male fetus had a der(22) chromosome--that is, he was trisomic for a...

Trisomy 14q-.

Birth defects original article series

Fawcett WA, McCord WK, Francke U.
PMID: 1218218
Birth Defects Orig Artic Ser. 1975;11(5):223-8.

Trisomy 14q- syndrome is relatively new and needs further delineation. In comparing our case with other reported cases (Table 1), some similarities are seen. Although the comparison of our case of partial trisomy 14 with the other cases reported...

Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19.

Cytogenetics and cell genetics

Naylor S, Lalouel JM, Shaw DJ.
PMID: 3864596
Cytogenet Cell Genet. 1985;40(1):242-67. doi: 10.1159/000132176.

No abstract available.

[A small supernumerary metacentric chromosome: interprétation test (author's transl)].

Journal de genetique humaine

Ayraud N, Noel B, Llyod M, Letourneau J, Martinon J.
PMID: 965953
J Genet Hum. 1976 Jun;24(2):81-93.

The report relates to a new case of small supernumerary metacentric chromosome. The phenotypical variability of previously published cases suggests that this chromosomal anomaly may arise from multiple origins. Our study shows the difficulties of a cytogenetic interpretation and...

Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19.

Somatic cell and molecular genetics

Gartler SM, Riley DE, Lebo RV, Cheung MC, Eddy RL, Shows TB.
PMID: 3016919
Somat Cell Mol Genet. 1986 Jul;12(4):395-401. doi: 10.1007/BF01570734.

In order to map human PGK sequences, DNA was prepared from 55 human-mouse somatic cell lines. The DNA was digested to completion with HindIII and Southern filters prepared. These filters were hybridized at high stringency conditions to a human...

Showing 1 to 12 of 589 entries