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Showing 1 to 12 of 1878 entries
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[Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes].

Genetika

Tsvetkova TG, Iankova MF.
PMID: 91543
Genetika. 1979;15(10):1870-9.

C-stained polymorphic variants of chromosomes 1, 9, 13--16, 21, 22 and Y were studied in married couples with reproductive failure (200 individuals) and in control couples having normal children and no spontaneous abortions and stillbirths. Location of heterochromatic segments,...

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Tsvetkova TG, Iankova MF. Khromosomnyĭ polimorfizm i narushenie reproduktivnoĭ funktsii u cheloveka. Soobshchenie II. C-varianty khromosom. [Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes]. Genetika. 1979;15(10):1870-9
Tsvetkova, T. G., & Iankova, M. F. (1979). Khromosomnyĭ polimorfizm i narushenie reproduktivnoĭ funktsii u cheloveka. Soobshchenie II. C-varianty khromosom. [Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes]. Genetika, 15(10), 1870-9.
Tsvetkova, T G, and Iankova, M F. "Khromosomnyĭ polimorfizm i narushenie reproduktivnoĭ funktsii u cheloveka. Soobshchenie II. C-varianty khromosom." [Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes]. Genetika vol. 15,10 (1979): 1870-9.
Tsvetkova TG, Iankova MF. Khromosomnyĭ polimorfizm i narushenie reproduktivnoĭ funktsii u cheloveka. Soobshchenie II. C-varianty khromosom. [Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes]. Genetika. 1979;15(10):1870-9. Russian. PMID: 91543.
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Unusual translocations in Ph1-positive acute lymphoblastic leukaemia.

Lancet (London, England)

Pittman S, Catovsky D, Morilla R.
PMID: 87666
Lancet. 1979 May 05;1(8123):986. doi: 10.1016/s0140-6736(79)91774-4.

No abstract available.

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Pittman S, Catovsky D, Morilla R. Unusual translocations in Ph1-positive acute lymphoblastic leukaemia. Lancet. 1979;1(8123):986doi: 10.1016/s0140-6736(79)91774-4.
Pittman, S., Catovsky, D., & Morilla, R. (1979). Unusual translocations in Ph1-positive acute lymphoblastic leukaemia. Lancet (London, England), 1(8123), 986. https://doi.org/10.1016/s0140-6736(79)91774-4
Pittman, S, et al. "Unusual translocations in Ph1-positive acute lymphoblastic leukaemia." Lancet (London, England) vol. 1,8123 (1979): 986. doi: https://doi.org/10.1016/s0140-6736(79)91774-4
Pittman S, Catovsky D, Morilla R. Unusual translocations in Ph1-positive acute lymphoblastic leukaemia. Lancet. 1979 May 05;1(8123):986. doi: 10.1016/s0140-6736(79)91774-4. PMID: 87666.
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Non-randomness in complex translocations of chronic myeloid leukaemia.

Scandinavian journal of haematology

Berger R, Bernheim A.
PMID: 282661
Scand J Haematol. 1978 Nov;21(5):418-20. doi: 10.1111/j.1600-0609.1978.tb00388.x.

A new case of chronic myeloid leukaemia with a complex translocation involving chromosomes No. 1, 9 and 22 is reported. The striking similarity of this case with another previously reported case and the involvement of band 9q34 in chromosome...

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Berger R, Bernheim A. Non-randomness in complex translocations of chronic myeloid leukaemia. Scand J Haematol. 1978;21(5):418-20doi: 10.1111/j.1600-0609.1978.tb00388.x.
Berger, R., & Bernheim, A. (1978). Non-randomness in complex translocations of chronic myeloid leukaemia. Scandinavian journal of haematology, 21(5), 418-20. https://doi.org/10.1111/j.1600-0609.1978.tb00388.x
Berger, R, and Bernheim, A. "Non-randomness in complex translocations of chronic myeloid leukaemia." Scandinavian journal of haematology vol. 21,5 (1978): 418-20. doi: https://doi.org/10.1111/j.1600-0609.1978.tb00388.x
Berger R, Bernheim A. Non-randomness in complex translocations of chronic myeloid leukaemia. Scand J Haematol. 1978 Nov;21(5):418-20. doi: 10.1111/j.1600-0609.1978.tb00388.x. PMID: 282661.
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Precise mapping of genes for phosphoglucomutase-1 and uridine monophosphate kinase on the short arm of human chromosome 1.

Cytogenetics and cell genetics

Francke U, George DL.
PMID: 222544
Cytogenet Cell Genet. 1978;22(1):384-8. doi: 10.1159/000130978.

No abstract available.

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Francke U, George DL. Precise mapping of genes for phosphoglucomutase-1 and uridine monophosphate kinase on the short arm of human chromosome 1. Cytogenet Cell Genet. 1978;22(1):384-8doi: 10.1159/000130978.
Francke, U., & George, D. L. (1978). Precise mapping of genes for phosphoglucomutase-1 and uridine monophosphate kinase on the short arm of human chromosome 1. Cytogenetics and cell genetics, 22(1), 384-8. https://doi.org/10.1159/000130978
Francke, U, and George, D L. "Precise mapping of genes for phosphoglucomutase-1 and uridine monophosphate kinase on the short arm of human chromosome 1." Cytogenetics and cell genetics vol. 22,1 (1978): 384-8. doi: https://doi.org/10.1159/000130978
Francke U, George DL. Precise mapping of genes for phosphoglucomutase-1 and uridine monophosphate kinase on the short arm of human chromosome 1. Cytogenet Cell Genet. 1978;22(1):384-8. doi: 10.1159/000130978. PMID: 222544.
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Trisomy 1q in polycythemia vera and its relation to disease transition.

American journal of hematology

Swolin B, Weinfeld A, Westin J.
PMID: 3706291
Am J Hematol. 1986 Jun;22(2):155-67. doi: 10.1002/ajh.2830220206.

Clinical and cytogenetic details of 12 patients with polycythemia vera and complete or partial trisomy of the long arm of chromosome 1 are reported. All patients had trisomy for at least the segments 1q22 to 1qter. The 1q or...

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Swolin B, Weinfeld A, Westin J. Trisomy 1q in polycythemia vera and its relation to disease transition. Am J Hematol. 1986;22(2):155-67doi: 10.1002/ajh.2830220206.
Swolin, B., Weinfeld, A., & Westin, J. (1986). Trisomy 1q in polycythemia vera and its relation to disease transition. American journal of hematology, 22(2), 155-67. https://doi.org/10.1002/ajh.2830220206
Swolin, B, et al. "Trisomy 1q in polycythemia vera and its relation to disease transition." American journal of hematology vol. 22,2 (1986): 155-67. doi: https://doi.org/10.1002/ajh.2830220206
Swolin B, Weinfeld A, Westin J. Trisomy 1q in polycythemia vera and its relation to disease transition. Am J Hematol. 1986 Jun;22(2):155-67. doi: 10.1002/ajh.2830220206. PMID: 3706291.
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Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions.

Cancer

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>3.0.co;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...

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Kakati S, Hayata I, Oshimura M, et al. Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions. Cancer. 1975;36(5):1729-38doi: 10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#.
Kakati, S., Hayata, I., Oshimura, M., & Sandberg, A. A. (1975). Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions. Cancer, 36(5), 1729-38. https://doi.org/10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#
Kakati, S, et al. "Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions." Cancer vol. 36,5 (1975): 1729-38. doi: https://doi.org/10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#
Kakati S, Hayata I, Oshimura M, Sandberg AA. Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions. Cancer. 1975 Nov;36(5):1729-38. doi: 10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#. PMID: 1192362.
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Human gene mapping. 2. Rotterdam Conference (1974). 2d International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 1 and 2.

Cytogenetics and cell genetics

[No authors listed]
PMID: 1192785
Cytogenet Cell Genet. 1975;14(3):173-82. doi: 10.1159/000130341.

No abstract available.

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Human gene mapping. 2. Rotterdam Conference (1974). 2d International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 1 and 2. Cytogenet Cell Genet. 1975;14(3):173-82doi: 10.1159/000130341.
(1975). Human gene mapping. 2. Rotterdam Conference (1974). 2d International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 1 and 2. Cytogenetics and cell genetics, 14(3), 173-82. https://doi.org/10.1159/000130341
"Human gene mapping. 2. Rotterdam Conference (1974). 2d International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 1 and 2." Cytogenetics and cell genetics vol. 14,3 (1975): 173-82. doi: https://doi.org/10.1159/000130341
Human gene mapping. 2. Rotterdam Conference (1974). 2d International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 1 and 2. Cytogenet Cell Genet. 1975;14(3):173-82. doi: 10.1159/000130341. PMID: 1192785.
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Regional mapping of human chromosomes 1 and 11.

Cytogenetics and cell genetics

Grzeschik KH.
PMID: 1192812
Cytogenet Cell Genet. 1975;14(3):342-5. doi: 10.1159/000130378.

No abstract available.

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Grzeschik KH. Regional mapping of human chromosomes 1 and 11. Cytogenet Cell Genet. 1975;14(3):342-5doi: 10.1159/000130378.
Grzeschik, K. H. (1975). Regional mapping of human chromosomes 1 and 11. Cytogenetics and cell genetics, 14(3), 342-5. https://doi.org/10.1159/000130378
Grzeschik, K H. "Regional mapping of human chromosomes 1 and 11." Cytogenetics and cell genetics vol. 14,3 (1975): 342-5. doi: https://doi.org/10.1159/000130378
Grzeschik KH. Regional mapping of human chromosomes 1 and 11. Cytogenet Cell Genet. 1975;14(3):342-5. doi: 10.1159/000130378. PMID: 1192812.
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[Chromosomal deviations in the genesis of reproductive failures].

Akusherstvo i ginekologiia

Georgieva V, Ganev V, Simeonova M, Lozanova T.
PMID: 3728858
Akush Ginekol (Sofiia). 1986;25(1):64-7.

No abstract available.

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Georgieva V, Ganev V, Simeonova M, et al. Khromozomni otkloneniia v genezata na reproduktivni neblagopoluchiia. [Chromosomal deviations in the genesis of reproductive failures]. Akush Ginekol (Sofiia). 1986;25(1):64-7
Georgieva, V., Ganev, V., Simeonova, M., & Lozanova, T. (1986). Khromozomni otkloneniia v genezata na reproduktivni neblagopoluchiia. [Chromosomal deviations in the genesis of reproductive failures]. Akusherstvo i ginekologiia, 25(1), 64-7.
Georgieva, V, et al. "Khromozomni otkloneniia v genezata na reproduktivni neblagopoluchiia." [Chromosomal deviations in the genesis of reproductive failures]. Akusherstvo i ginekologiia vol. 25,1 (1986): 64-7.
Georgieva V, Ganev V, Simeonova M, Lozanova T. Khromozomni otkloneniia v genezata na reproduktivni neblagopoluchiia. [Chromosomal deviations in the genesis of reproductive failures]. Akush Ginekol (Sofiia). 1986;25(1):64-7. Bulgarian. PMID: 3728858.
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Cytological studies of tumors. XLIX. Chronic lymphocytic leukemia with A1-G chromosome translocation and high serum gamma-globulin production.

Gan

Obara Y, Makino S, Mikuni C.
PMID: 4192022
Gan. 1970 Feb;61(1):1-6.

No abstract available.

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Obara Y, Makino S, Mikuni C. Cytological studies of tumors. XLIX. Chronic lymphocytic leukemia with A1-G chromosome translocation and high serum gamma-globulin production. Gan. 1970;61(1):1-6
Obara, Y., Makino, S., & Mikuni, C. (1970). Cytological studies of tumors. XLIX. Chronic lymphocytic leukemia with A1-G chromosome translocation and high serum gamma-globulin production. Gan, 61(1), 1-6.
Obara, Y, et al. "Cytological studies of tumors. XLIX. Chronic lymphocytic leukemia with A1-G chromosome translocation and high serum gamma-globulin production." Gan vol. 61,1 (1970): 1-6.
Obara Y, Makino S, Mikuni C. Cytological studies of tumors. XLIX. Chronic lymphocytic leukemia with A1-G chromosome translocation and high serum gamma-globulin production. Gan. 1970 Feb;61(1):1-6. PMID: 4192022.
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[Union of 2 carriers of a balanced translocation. Familial study of 3 generations].

Annales de genetique

Gilgenkrantz S, Grégoire MJ, Chery M, Defèche C.
PMID: 3879150
Ann Genet. 1985;28(3):164-6.

Both unrelated members of a couple are carrier of a balanced translocation, a reciprocal and a Robertsonian translocation, respectively. After reporting on the family investigation of these individuals, the authors analyse the offspring of six other similar couples reported...

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Gilgenkrantz S, Grégoire MJ, Chery M, et al. Union de deux porteurs de translocation équilibrée. Etude familiale sur trois générations. [Union of 2 carriers of a balanced translocation. Familial study of 3 generations]. Ann Genet. 1985;28(3):164-6
Gilgenkrantz, S., Grégoire, M. J., Chery, M., & Defèche, C. (1985). Union de deux porteurs de translocation équilibrée. Etude familiale sur trois générations. [Union of 2 carriers of a balanced translocation. Familial study of 3 generations]. Annales de genetique, 28(3), 164-6.
Gilgenkrantz, S, et al. "Union de deux porteurs de translocation équilibrée. Etude familiale sur trois générations." [Union of 2 carriers of a balanced translocation. Familial study of 3 generations]. Annales de genetique vol. 28,3 (1985): 164-6.
Gilgenkrantz S, Grégoire MJ, Chery M, Defèche C. Union de deux porteurs de translocation équilibrée. Etude familiale sur trois générations. [Union of 2 carriers of a balanced translocation. Familial study of 3 generations]. Ann Genet. 1985;28(3):164-6. French. PMID: 3879150.
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Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus.

Humangenetik

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

No abstract available.

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Kim MA. Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus. Humangenetik. 1974;21(4):331-40doi: 10.1007/BF00273371.
Kim, M. A. (1974). Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus. Humangenetik, 21(4), 331-40. https://doi.org/10.1007/BF00273371
Kim, M A. "Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus." Humangenetik vol. 21,4 (1974): 331-40. doi: https://doi.org/10.1007/BF00273371
Kim MA. Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus. Humangenetik. 1974 Mar 28;21(4):331-40. doi: 10.1007/BF00273371. PMID: 4837300.
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Showing 1 to 12 of 1878 entries