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The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes.

Human genetics

Podugolnikova OA.
PMID: 478535
Hum Genet. 1979 Jul 18;49(3):261-8. doi: 10.1007/BF00569345.

The correlation relationship of the lengths of C segments on chromosomes 1, 9, 16, and Y was studied in a group of normal boys and girls (50 boys and 50 girls). No correlation was found between the C segment...

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Podugolnikova OA. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes. Hum Genet. 1979;49(3):261-8doi: 10.1007/BF00569345.
Podugolnikova, O. A. (1979). The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes. Human genetics, 49(3), 261-8. https://doi.org/10.1007/BF00569345
Podugolnikova, O A. "The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes." Human genetics vol. 49,3 (1979): 261-8. doi: https://doi.org/10.1007/BF00569345
Podugolnikova OA. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes. Hum Genet. 1979 Jul 18;49(3):261-8. doi: 10.1007/BF00569345. PMID: 478535.
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A case of gouty arthritis associated with Down's syndrome.

Journal of mental deficiency research

Nishida Y, Akaoka I, Nishizawa T, Maruki M, Aikawa T, Mitamura T, Yokohari R, Horiuchi Y.
PMID: 137983
J Ment Defic Res. 1976 Dec;20(4):277-83. doi: 10.1111/j.1365-2788.1976.tb00954.x.

Gouty arthritis developed in a twenty-one-year-old male whose karyotyping showed Trisomy 21. His serum urate level was 13.1 mg per 100 ml and his twenty-four-hour urinary uric acid excretion was 431 mg on a low purine diet. Uric acid...

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Nishida Y, Akaoka I, Nishizawa T, et al. A case of gouty arthritis associated with Down's syndrome. J Ment Defic Res. 1976;20(4):277-83doi: 10.1111/j.1365-2788.1976.tb00954.x.
Nishida, Y., Akaoka, I., Nishizawa, T., Maruki, M., Aikawa, T., Mitamura, T., Yokohari, R., & Horiuchi, Y. (1976). A case of gouty arthritis associated with Down's syndrome. Journal of mental deficiency research, 20(4), 277-83. https://doi.org/10.1111/j.1365-2788.1976.tb00954.x
Nishida, Y, et al. "A case of gouty arthritis associated with Down's syndrome." Journal of mental deficiency research vol. 20,4 (1976): 277-83. doi: https://doi.org/10.1111/j.1365-2788.1976.tb00954.x
Nishida Y, Akaoka I, Nishizawa T, Maruki M, Aikawa T, Mitamura T, Yokohari R, Horiuchi Y. A case of gouty arthritis associated with Down's syndrome. J Ment Defic Res. 1976 Dec;20(4):277-83. doi: 10.1111/j.1365-2788.1976.tb00954.x. PMID: 137983.
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Genetic and epidemiologic investigation of spontaneous abortion: relevance to clinical practice.

Birth defects original article series

Warburton D, Susser M, Stein Z, Kline J.
PMID: 508914
Birth Defects Orig Artic Ser. 1979;15(5):127-36.

No abstract available.

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Warburton D, Susser M, Stein Z, et al. Genetic and epidemiologic investigation of spontaneous abortion: relevance to clinical practice. Birth Defects Orig Artic Ser. 1979;15(5):127-36
Warburton, D., Susser, M., Stein, Z., & Kline, J. (1979). Genetic and epidemiologic investigation of spontaneous abortion: relevance to clinical practice. Birth defects original article series, 15(5), 127-36.
Warburton, D, et al. "Genetic and epidemiologic investigation of spontaneous abortion: relevance to clinical practice." Birth defects original article series vol. 15,5 (1979): 127-36.
Warburton D, Susser M, Stein Z, Kline J. Genetic and epidemiologic investigation of spontaneous abortion: relevance to clinical practice. Birth Defects Orig Artic Ser. 1979;15(5):127-36. PMID: 508914.
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17 long arm isochromosome. A common anomaly in malignat blood disorders.

Annales de genetique

Engel E, McKee LC, Flexner JM, McGee BJ.
PMID: 50044
Ann Genet. 1975 Mar;18(1):56-60.

A cytogenetic anomaly consisting in the replacement of a 17 by its long arm isochromosome was identified as the only alteration in the marrow cells of two patients with acute granulocytic leukemia. In one case, the specific nature of...

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Engel E, McKee LC, Flexner JM, et al. 17 long arm isochromosome. A common anomaly in malignat blood disorders. Ann Genet. 1975;18(1):56-60
Engel, E., McKee, L. C., Flexner, J. M., & McGee, B. J. (1975). 17 long arm isochromosome. A common anomaly in malignat blood disorders. Annales de genetique, 18(1), 56-60.
Engel, E, et al. "17 long arm isochromosome. A common anomaly in malignat blood disorders." Annales de genetique vol. 18,1 (1975): 56-60.
Engel E, McKee LC, Flexner JM, McGee BJ. 17 long arm isochromosome. A common anomaly in malignat blood disorders. Ann Genet. 1975 Mar;18(1):56-60. PMID: 50044.
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Karyotype and chromosomal banding pattern in Heteropeza pygmaea.

Chromosoma

Fantes J, Camenzind R.
PMID: 50166
Chromosoma. 1975;50(4):421-9. doi: 10.1007/BF00327077.

The chromosomes of somatic and germ line cells of female embryos produced by paedogenesis were studied. The haploid set in somatic cells consists of one long submetacentric chromosome, one large acrocentric, one medium metacentric and two small acrocentrics. The...

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Fantes J, Camenzind R. Karyotype and chromosomal banding pattern in Heteropeza pygmaea. Chromosoma. 1975;50(4):421-9doi: 10.1007/BF00327077.
Fantes, J., & Camenzind, R. (1975). Karyotype and chromosomal banding pattern in Heteropeza pygmaea. Chromosoma, 50(4), 421-9. https://doi.org/10.1007/BF00327077
Fantes, J, and Camenzind, R. "Karyotype and chromosomal banding pattern in Heteropeza pygmaea." Chromosoma vol. 50,4 (1975): 421-9. doi: https://doi.org/10.1007/BF00327077
Fantes J, Camenzind R. Karyotype and chromosomal banding pattern in Heteropeza pygmaea. Chromosoma. 1975;50(4):421-9. doi: 10.1007/BF00327077. PMID: 50166.
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[Structural abnormalities of the Y chromosome. Observations in ten cases].

Journal de genetique humaine

Mattei JF, Mattei MG, Lucas C, Giraud F.
PMID: 479854
J Genet Hum. 1979 Mar;27(1):53-66.

The authors report ten cases of structural anomalies involving the Y chromosome: five cases of a dicentric Y chromosome, one ring Y chromosome, one case of a Y isochromosome containing the long arms, one deletion of the long arms...

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Mattei JF, Mattei MG, Lucas C, et al. Les anomalies de structure du chromosome Y -- a propos de 10 observations. [Structural abnormalities of the Y chromosome. Observations in ten cases]. J Genet Hum. 1979;27(1):53-66
Mattei, J. F., Mattei, M. G., Lucas, C., & Giraud, F. (1979). Les anomalies de structure du chromosome Y -- a propos de 10 observations. [Structural abnormalities of the Y chromosome. Observations in ten cases]. Journal de genetique humaine, 27(1), 53-66.
Mattei, J F, et al. "Les anomalies de structure du chromosome Y -- a propos de 10 observations." [Structural abnormalities of the Y chromosome. Observations in ten cases]. Journal de genetique humaine vol. 27,1 (1979): 53-66.
Mattei JF, Mattei MG, Lucas C, Giraud F. Les anomalies de structure du chromosome Y -- a propos de 10 observations. [Structural abnormalities of the Y chromosome. Observations in ten cases]. J Genet Hum. 1979 Mar;27(1):53-66. French. PMID: 479854.
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Prenatal detection of the 47, XYY karyotype.

Lancet (London, England)

Goldenberg RL, Finley SC.
PMID: 79819
Lancet. 1978 Aug 26;2(8087):465-6. doi: 10.1016/s0140-6736(78)91458-7.

The ethical decisions involved before and after the prenatal diagnosis of a 47, XYY karyotype in the fetus of a 32-year-old woman are discussed. It was decided that the parents should be presented with all the known facts about...

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Goldenberg RL, Finley SC. Prenatal detection of the 47, XYY karyotype. Lancet. 1978;2(8087):465-6doi: 10.1016/s0140-6736(78)91458-7.
Goldenberg, R. L., & Finley, S. C. (1978). Prenatal detection of the 47, XYY karyotype. Lancet (London, England), 2(8087), 465-6. https://doi.org/10.1016/s0140-6736(78)91458-7
Goldenberg, R L, and Finley, S C. "Prenatal detection of the 47, XYY karyotype." Lancet (London, England) vol. 2,8087 (1978): 465-6. doi: https://doi.org/10.1016/s0140-6736(78)91458-7
Goldenberg RL, Finley SC. Prenatal detection of the 47, XYY karyotype. Lancet. 1978 Aug 26;2(8087):465-6. doi: 10.1016/s0140-6736(78)91458-7. PMID: 79819.
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Giemsa banding patterns in chronic lymphocytic leukaemia.

Humangenetik

Crossen PE.
PMID: 50272
Humangenetik. 1975;27(2):151-6.

The banding patterns of chromosomes from 20 patients with chronic lymphocytic leukaemia (C.L.L.) have been analyzed. 97 of 100 metaphases examined had a normal banding pattern. The 3 remaining metaphases, all from one patient had bands similar to those...

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Crossen PE. Giemsa banding patterns in chronic lymphocytic leukaemia. Humangenetik. 1975;27(2):151-6
Crossen, P. E. (1975). Giemsa banding patterns in chronic lymphocytic leukaemia. Humangenetik, 27(2), 151-6.
Crossen, P E. "Giemsa banding patterns in chronic lymphocytic leukaemia." Humangenetik vol. 27,2 (1975): 151-6.
Crossen PE. Giemsa banding patterns in chronic lymphocytic leukaemia. Humangenetik. 1975;27(2):151-6. PMID: 50272.
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Karyological instability of neoplastic somatic cells.

In vitro

DiPaolo JA.
PMID: 50282
In Vitro. 1975 Mar-Apr;11(2):89-96. doi: 10.1007/BF02624081.

No abstract available.

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DiPaolo JA. Karyological instability of neoplastic somatic cells. In Vitro. 1975;11(2):89-96doi: 10.1007/BF02624081.
DiPaolo, J. A. (1975). Karyological instability of neoplastic somatic cells. In vitro, 11(2), 89-96. https://doi.org/10.1007/BF02624081
DiPaolo, J A. "Karyological instability of neoplastic somatic cells." In vitro vol. 11,2 (1975): 89-96. doi: https://doi.org/10.1007/BF02624081
DiPaolo JA. Karyological instability of neoplastic somatic cells. In Vitro. 1975 Mar-Apr;11(2):89-96. doi: 10.1007/BF02624081. PMID: 50282.
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Specific cellular defects in patients with Fanconi anemia.

Journal of cellular physiology

Weksberg R, Buchwald M, Sargent P, Thompson MW, Siminovitch L.
PMID: 511954
J Cell Physiol. 1979 Nov;101(2):311-23. doi: 10.1002/jcp.1041010211.

Measurements of plating efficiency, accumulation of metaphases and generation times have shown that fibroblast from patients with Fanconi anemia (FA) have decreased probability of completing a further division after successful mitosis. Thus FA cells show decreased growth rates and...

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Weksberg R, Buchwald M, Sargent P, et al. Specific cellular defects in patients with Fanconi anemia. J Cell Physiol. 1979;101(2):311-23doi: 10.1002/jcp.1041010211.
Weksberg, R., Buchwald, M., Sargent, P., Thompson, M. W., & Siminovitch, L. (1979). Specific cellular defects in patients with Fanconi anemia. Journal of cellular physiology, 101(2), 311-23. https://doi.org/10.1002/jcp.1041010211
Weksberg, R, et al. "Specific cellular defects in patients with Fanconi anemia." Journal of cellular physiology vol. 101,2 (1979): 311-23. doi: https://doi.org/10.1002/jcp.1041010211
Weksberg R, Buchwald M, Sargent P, Thompson MW, Siminovitch L. Specific cellular defects in patients with Fanconi anemia. J Cell Physiol. 1979 Nov;101(2):311-23. doi: 10.1002/jcp.1041010211. PMID: 511954.
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[Sex ratio and survival rate in embryogenesis and the perinatal period].

TSitologiia i genetika

Golovachev GD, Novikova LN.
PMID: 483389
Tsitol Genet. 1979 Mar-Apr;13(3):213-5.

Sex ratio was studied among abortuses and infants who died perinatally (9972 cases). Sex begins influencing mortality in the perinatal period, in which a significant increase in the sex ratio is shown (106 males: 100 females--antenatal; 136 males: 100...

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Golovachev GD, Novikova LN. Sootnoshenie i vyzhivaemost' polov v émbriogeneze i perinatal'nom periode. [Sex ratio and survival rate in embryogenesis and the perinatal period]. Tsitol Genet. 1979;13(3):213-5
Golovachev, G. D., & Novikova, L. N. (1979). Sootnoshenie i vyzhivaemost' polov v émbriogeneze i perinatal'nom periode. [Sex ratio and survival rate in embryogenesis and the perinatal period]. TSitologiia i genetika, 13(3), 213-5.
Golovachev, G D, and Novikova, L N. "Sootnoshenie i vyzhivaemost' polov v émbriogeneze i perinatal'nom periode." [Sex ratio and survival rate in embryogenesis and the perinatal period]. TSitologiia i genetika vol. 13,3 (1979): 213-5.
Golovachev GD, Novikova LN. Sootnoshenie i vyzhivaemost' polov v émbriogeneze i perinatal'nom periode. [Sex ratio and survival rate in embryogenesis and the perinatal period]. Tsitol Genet. 1979 Mar-Apr;13(3):213-5. Russian. PMID: 483389.
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Determination of the primitive karyotype for Peromyscus.

Journal of mammalogy

Greenbaum IF, Baker RJ.
PMID: 750637
J Mammal. 1978 Nov;59(4):820-34.

No abstract available.

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Greenbaum IF, Baker RJ. Determination of the primitive karyotype for Peromyscus. J Mammal. 1978;59(4):820-34
Greenbaum, I. F., & Baker, R. J. (1978). Determination of the primitive karyotype for Peromyscus. Journal of mammalogy, 59(4), 820-34.
Greenbaum, I F, and Baker, R J. "Determination of the primitive karyotype for Peromyscus." Journal of mammalogy vol. 59,4 (1978): 820-34.
Greenbaum IF, Baker RJ. Determination of the primitive karyotype for Peromyscus. J Mammal. 1978 Nov;59(4):820-34. PMID: 750637.
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Showing 1 to 12 of 49274 entries