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Showing 1 to 12 of 7659 entries
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Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins?.

Cancer genetics and cytogenetics

Harnett PR, Kearsley JH, Hayward NK, Dracopoli NC, Kefford RF.
PMID: 1676609
Cancer Genet Cytogenet. 1991 Jul 01;54(1):109-13. doi: 10.1016/0165-4608(91)90037-u.

The location of genes involved in tumor evolution has been inferred from experiments in which loss of constitutional heterozygosity has been detected in tumor DNA at high frequency in specific chromosome regions. For example, cytogenetic and molecular abnormalities on...

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Harnett PR, Kearsley JH, Hayward NK, et al. Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins?. Cancer Genet Cytogenet. 1991;54(1):109-13doi: 10.1016/0165-4608(91)90037-u.
Harnett, P. R., Kearsley, J. H., Hayward, N. K., Dracopoli, N. C., & Kefford, R. F. (1991). Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins?. Cancer genetics and cytogenetics, 54(1), 109-13. https://doi.org/10.1016/0165-4608(91)90037-u
Harnett, P R, et al. "Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins?." Cancer genetics and cytogenetics vol. 54,1 (1991): 109-13. doi: https://doi.org/10.1016/0165-4608(91)90037-u
Harnett PR, Kearsley JH, Hayward NK, Dracopoli NC, Kefford RF. Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins?. Cancer Genet Cytogenet. 1991 Jul 01;54(1):109-13. doi: 10.1016/0165-4608(91)90037-u. PMID: 1676609.
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Child with deletion of 4q and duplication of 1q.

American journal of medical genetics

Wade J, Morgan T, Allanson J.
PMID: 2596517
Am J Med Genet. 1989 Aug;33(4):553-4. doi: 10.1002/ajmg.1320330430.

No abstract available.

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Wade J, Morgan T, Allanson J. Child with deletion of 4q and duplication of 1q. Am J Med Genet. 1989;33(4):553-4doi: 10.1002/ajmg.1320330430.
Wade, J., Morgan, T., & Allanson, J. (1989). Child with deletion of 4q and duplication of 1q. American journal of medical genetics, 33(4), 553-4. https://doi.org/10.1002/ajmg.1320330430
Wade, J, et al. "Child with deletion of 4q and duplication of 1q." American journal of medical genetics vol. 33,4 (1989): 553-4. doi: https://doi.org/10.1002/ajmg.1320330430
Wade J, Morgan T, Allanson J. Child with deletion of 4q and duplication of 1q. Am J Med Genet. 1989 Aug;33(4):553-4. doi: 10.1002/ajmg.1320330430. PMID: 2596517.
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Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2.

American journal of medical genetics

Clark RD, Fenner-Gonzales M.
PMID: 2596530
Am J Med Genet. 1989 Nov;34(3):422-6. doi: 10.1002/ajmg.1320340319.

We report on a newborn boy with manifestations of Fryns syndrome who also had a mosaic tandem duplication of chromosome 1q24-31.2. The child had a diaphragmatic hernia, cleft palate, hypoplastic and absent digits, micrognathia, long philtrum, thin upper lip,...

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Clark RD, Fenner-Gonzales M. Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2. Am J Med Genet. 1989;34(3):422-6doi: 10.1002/ajmg.1320340319.
Clark, R. D., & Fenner-Gonzales, M. (1989). Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2. American journal of medical genetics, 34(3), 422-6. https://doi.org/10.1002/ajmg.1320340319
Clark, R D, and Fenner-Gonzales, M. "Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2." American journal of medical genetics vol. 34,3 (1989): 422-6. doi: https://doi.org/10.1002/ajmg.1320340319
Clark RD, Fenner-Gonzales M. Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2. Am J Med Genet. 1989 Nov;34(3):422-6. doi: 10.1002/ajmg.1320340319. PMID: 2596530.
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1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer.

Genes, chromosomes & cancer

Mitchell EL, Santibanez-Koref MF.
PMID: 2268577
Genes Chromosomes Cancer. 1990 Nov;2(4):278-89. doi: 10.1002/gcc.2870020405.

Cytogenetic data on 14 breast carcinomas were examined to determine which chromosome arms and bands are preferentially involved in structural chromosome changes. Chromosome arms 17p, 16q, and 1p and band 1p13 were found to be significantly involved. A review...

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Mitchell EL, Santibanez-Koref MF. 1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer. Genes Chromosomes Cancer. 1990;2(4):278-89doi: 10.1002/gcc.2870020405.
Mitchell, E. L., & Santibanez-Koref, M. F. (1990). 1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer. Genes, chromosomes & cancer, 2(4), 278-89. https://doi.org/10.1002/gcc.2870020405
Mitchell, E L, and Santibanez-Koref, M F. "1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer." Genes, chromosomes & cancer vol. 2,4 (1990): 278-89. doi: https://doi.org/10.1002/gcc.2870020405
Mitchell EL, Santibanez-Koref MF. 1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer. Genes Chromosomes Cancer. 1990 Nov;2(4):278-89. doi: 10.1002/gcc.2870020405. PMID: 2268577.
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A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q.

American journal of medical genetics

Halal F, Vekemans M, Der Kaloustian VM.
PMID: 2658588
Am J Med Genet. 1989 Mar;32(3):376-9. doi: 10.1002/ajmg.1320320322.

Here we report on a girl with a translocation between 1 and 2 and duplication 1p and deletion 2q resulting in a multiple congenital anomaly syndrome including intrauterine growth retardation, microcephaly, hypotelorism, cleft palate, subglottic stenosis, umbilical hernia, scoliosis,...

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Halal F, Vekemans M, Der Kaloustian VM. A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q. Am J Med Genet. 1989;32(3):376-9doi: 10.1002/ajmg.1320320322.
Halal, F., Vekemans, M., & Der Kaloustian, V. M. (1989). A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q. American journal of medical genetics, 32(3), 376-9. https://doi.org/10.1002/ajmg.1320320322
Halal, F, et al. "A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q." American journal of medical genetics vol. 32,3 (1989): 376-9. doi: https://doi.org/10.1002/ajmg.1320320322
Halal F, Vekemans M, Der Kaloustian VM. A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q. Am J Med Genet. 1989 Mar;32(3):376-9. doi: 10.1002/ajmg.1320320322. PMID: 2658588.
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The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation.

Human genetics

Estop AM, Levinson F, Cieply K, Vankirk V.
PMID: 1618491
Hum Genet. 1992 Jun;89(4):425-9. doi: 10.1007/BF00194315.

We examined the meiotic segregation pattern of a t(1;4)(p36.2;q31.3) reciprocal translocation in two male cousins heterozygous for the translocation. The wife of subject 1 had four recognized spontaneous abortions and two carrier daughters, and the wife of subject 2...

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Estop AM, Levinson F, Cieply K, et al. The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation. Hum Genet. 1992;89(4):425-9doi: 10.1007/BF00194315.
Estop, A. M., Levinson, F., Cieply, K., & Vankirk, V. (1992). The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation. Human genetics, 89(4), 425-9. https://doi.org/10.1007/BF00194315
Estop, A M, et al. "The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation." Human genetics vol. 89,4 (1992): 425-9. doi: https://doi.org/10.1007/BF00194315
Estop AM, Levinson F, Cieply K, Vankirk V. The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation. Hum Genet. 1992 Jun;89(4):425-9. doi: 10.1007/BF00194315. PMID: 1618491.
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[Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency].

Ceskoslovenska pediatrie

Franková Y, Zeman J, Mejsnarová B, Stloukalová M, Pajerek J.
PMID: 2119894
Cesk Pediatr. 1990 Feb;45(2):87-8.

A six-month-old boy with partial trisomia 1q25-1q32. In the phenotype psychomotor retardation, progeric facial features and general dystrophy dominated. He failed to thrive partly because of milk intolerance due to hypolactasia. This disorder was revealed by histochemical examination of...

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Franková Y, Zeman J, Mejsnarová B, et al. Parciální trisomie 1q25-1q32 u chlapce s izolovaným deficitem laktázy. [Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency]. Cesk Pediatr. 1990;45(2):87-8
Franková, Y., Zeman, J., Mejsnarová, B., Stloukalová, M., & Pajerek, J. (1990). Parciální trisomie 1q25-1q32 u chlapce s izolovaným deficitem laktázy. [Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency]. Ceskoslovenska pediatrie, 45(2), 87-8.
Franková, Y, et al. "Parciální trisomie 1q25-1q32 u chlapce s izolovaným deficitem laktázy." [Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency]. Ceskoslovenska pediatrie vol. 45,2 (1990): 87-8.
Franková Y, Zeman J, Mejsnarová B, Stloukalová M, Pajerek J. Parciální trisomie 1q25-1q32 u chlapce s izolovaným deficitem laktázy. [Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency]. Cesk Pediatr. 1990 Feb;45(2):87-8. Czech. PMID: 2119894.
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Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes.

European journal of cell biology

Willecke K, Jungbluth S, Dahl E, Hennemann H, Heynkes R, Grzeschik KH.
PMID: 1964417
Eur J Cell Biol. 1990 Dec;53(2):275-80.

Connexin genes code for proteins that form cell-to-cell channels known as gap junctions. The genes for the known connexins 26, 32, 43, and 46 have been assigned to human chromosomes, 13, X, 6, and 13, respectively, by analysis of...

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Willecke K, Jungbluth S, Dahl E, et al. Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes. Eur J Cell Biol. 1990;53(2):275-80
Willecke, K., Jungbluth, S., Dahl, E., Hennemann, H., Heynkes, R., & Grzeschik, K. H. (1990). Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes. European journal of cell biology, 53(2), 275-80.
Willecke, K, et al. "Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes." European journal of cell biology vol. 53,2 (1990): 275-80.
Willecke K, Jungbluth S, Dahl E, Hennemann H, Heynkes R, Grzeschik KH. Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes. Eur J Cell Biol. 1990 Dec;53(2):275-80. PMID: 1964417.
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A translocation (1;10)(p32;q24) in a neuroblastoma cell line derived from marrow metastases.

Cancer genetics and cytogenetics

Skinnider L, Wang SY, Wang HC, Krespin HI.
PMID: 2302681
Cancer Genet Cytogenet. 1990 Mar;45(1):131-5. doi: 10.1016/0165-4608(90)90076-m.

Chromosomes of a cell line derived from neuroblastoma metastases were analysed. Ninety-nine percent of the cells had 46 chromosomes, and of 10 cells analysed by G-banding, all had a t(1;10)(p32;q24).

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Skinnider L, Wang SY, Wang HC, et al. A translocation (1;10)(p32;q24) in a neuroblastoma cell line derived from marrow metastases. Cancer Genet Cytogenet. 1990;45(1):131-5doi: 10.1016/0165-4608(90)90076-m.
Skinnider, L., Wang, S. Y., Wang, H. C., & Krespin, H. I. (1990). A translocation (1;10)(p32;q24) in a neuroblastoma cell line derived from marrow metastases. Cancer genetics and cytogenetics, 45(1), 131-5. https://doi.org/10.1016/0165-4608(90)90076-m
Skinnider, L, et al. "A translocation (1;10)(p32;q24) in a neuroblastoma cell line derived from marrow metastases." Cancer genetics and cytogenetics vol. 45,1 (1990): 131-5. doi: https://doi.org/10.1016/0165-4608(90)90076-m
Skinnider L, Wang SY, Wang HC, Krespin HI. A translocation (1;10)(p32;q24) in a neuroblastoma cell line derived from marrow metastases. Cancer Genet Cytogenet. 1990 Mar;45(1):131-5. doi: 10.1016/0165-4608(90)90076-m. PMID: 2302681.
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Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias.

Genes, chromosomes & cancer

Bernard O, Guglielmi P, Jonveaux P, Cherif D, Gisselbrecht S, Mauchauffe M, Berger R, Larsen CJ, Mathieu-Mahul D.
PMID: 1964581
Genes Chromosomes Cancer. 1990 Jan;1(3):194-208. doi: 10.1002/gcc.2870010303.

Molecular study of a t(1;14)(p32;q11) translocation found in an acute T-cell leukemia (Kd cells) with a relatively mature phenotype is reported. Complex DNA rearrangements were characterized in the TCR alpha/delta locus. Besides a productive V alpha/J alpha assembly found...

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Bernard O, Guglielmi P, Jonveaux P, et al. Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias. Genes Chromosomes Cancer. 1990;1(3):194-208doi: 10.1002/gcc.2870010303.
Bernard, O., Guglielmi, P., Jonveaux, P., Cherif, D., Gisselbrecht, S., Mauchauffe, M., Berger, R., Larsen, C. J., & Mathieu-Mahul, D. (1990). Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias. Genes, chromosomes & cancer, 1(3), 194-208. https://doi.org/10.1002/gcc.2870010303
Bernard, O, et al. "Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias." Genes, chromosomes & cancer vol. 1,3 (1990): 194-208. doi: https://doi.org/10.1002/gcc.2870010303
Bernard O, Guglielmi P, Jonveaux P, Cherif D, Gisselbrecht S, Mauchauffe M, Berger R, Larsen CJ, Mathieu-Mahul D. Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias. Genes Chromosomes Cancer. 1990 Jan;1(3):194-208. doi: 10.1002/gcc.2870010303. PMID: 1964581.
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Chromosome 1 studies in Wilms' tumor.

Cancer genetics and cytogenetics

McDowell H, Howard P, Martin J, Hart C, Crampton J.
PMID: 2557151
Cancer Genet Cytogenet. 1989 Dec;43(2):203-9. doi: 10.1016/0165-4608(89)90031-9.

Ten newly diagnosed patients with Wilms' tumor had blood and tumor samples taken for cytogenetic analysis. DNA was also extracted from these samples, along with blood obtained from both parents and an age- and sex-matched control. Molecular biological techniques...

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McDowell H, Howard P, Martin J, et al. Chromosome 1 studies in Wilms' tumor. Cancer Genet Cytogenet. 1989;43(2):203-9doi: 10.1016/0165-4608(89)90031-9.
McDowell, H., Howard, P., Martin, J., Hart, C., & Crampton, J. (1989). Chromosome 1 studies in Wilms' tumor. Cancer genetics and cytogenetics, 43(2), 203-9. https://doi.org/10.1016/0165-4608(89)90031-9
McDowell, H, et al. "Chromosome 1 studies in Wilms' tumor." Cancer genetics and cytogenetics vol. 43,2 (1989): 203-9. doi: https://doi.org/10.1016/0165-4608(89)90031-9
McDowell H, Howard P, Martin J, Hart C, Crampton J. Chromosome 1 studies in Wilms' tumor. Cancer Genet Cytogenet. 1989 Dec;43(2):203-9. doi: 10.1016/0165-4608(89)90031-9. PMID: 2557151.
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A dinucleotide repeat polymorphism at the D1S116 locus.

Nucleic acids research

Sharma V, Allen L, Magenis RE, Litt M.
PMID: 2020559
Nucleic Acids Res. 1991 Mar 11;19(5):1169.
Free PMC Article

No abstract available.

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Sharma V, Allen L, Magenis RE, et al. A dinucleotide repeat polymorphism at the D1S116 locus. Nucleic Acids Res. 1991;19(5):1169
Sharma, V., Allen, L., Magenis, R. E., & Litt, M. (1991). A dinucleotide repeat polymorphism at the D1S116 locus. Nucleic acids research, 19(5), 1169.
Sharma, V, et al. "A dinucleotide repeat polymorphism at the D1S116 locus." Nucleic acids research vol. 19,5 (1991): 1169.
Sharma V, Allen L, Magenis RE, Litt M. A dinucleotide repeat polymorphism at the D1S116 locus. Nucleic Acids Res. 1991 Mar 11;19(5):1169. PMID: 2020559; PMCID: PMC333827.
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Showing 1 to 12 of 7659 entries