 Chromosomes, Human, 6-12 and X
"Chromosomes, Human, 6-12 and X" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The medium-sized, submetacentric human chromosomes, called group C in the human chromosome classification. This group consists of chromosome pairs 6, 7, 8, 9, 10, 11, and 12 and the X chromosome.
| Descriptor ID |
D002906
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| MeSH Number(s) |
A11.284.187.520.300.325 G05.360.162.520.300.325
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 6-12 and X".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 6-12 and X".
- Chromosomes, Human, 6-12 and X
- Chromosomes, Human, Pair 10
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 12
- Chromosomes, Human, Pair 6
- Chromosomes, Human, Pair 7
- Chromosomes, Human, Pair 8
- Chromosomes, Human, Pair 9
- Chromosomes, Human, X
This graph shows the total number of publications written about "Chromosomes, Human, 6-12 and X" by people in this website by year, and whether "Chromosomes, Human, 6-12 and X" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 1 | 1 | | 2007 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, 6-12 and X" by people in Profiles.
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Kim JH, Dhanasekaran SM, Mehra R, Tomlins SA, Gu W, Yu J, Kumar-Sinha C, Cao X, Dash A, Wang L, Ghosh D, Shedden K, Montie JE, Rubin MA, Pienta KJ, Shah RB, Chinnaiyan AM. Integrative analysis of genomic aberrations associated with prostate cancer progression. Cancer Res. 2007 Sep 01; 67(17):8229-39.
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Morse HG, Moore GE, Ortiz LM, Gonzalez R, Robinson WA. Malignant melanoma: from subcutaneous nodule to brain metastasis. Cancer Genet Cytogenet. 1994 Jan; 72(1):16-23.
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Spritz RA, Mager D, Pauli RM, Laxova R. Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome. Am J Hum Genet. 1986 Aug; 39(2):265-73.
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Disteche CM, Swisshelm K, Forbes S, Pagon RA. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes. Hum Genet. 1984; 66(1):71-6.
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Chitambar CR, Robinson WA, Glode LM. Familial leukemia and aplastic anemia associated with monosomy 7. Am J Med. 1983 Nov; 75(5):756-62.
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Pauli RM, Kirkpatrick SJ, Meisner LF, Mijanovich JR, Spritz RA. Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocation. Clin Genet. 1982 Dec; 22(6):340-7.
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Swisshelm K, Rodriguez ML, Luthy D, Salk D, Norwood T. Antenatal diagnosis of mosaic trisomy 8 confirmed in fetal tissues. Clin Genet. 1981 Oct; 20(4):276-80.
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Spritz RA, Emanuel BS, Chern CJ, Mellman WJ. Gene dosage effect: intraband mapping of human soluble glutamic oxaloacetic transaminase. Cytogenet Cell Genet. 1979; 23(3):149-56.
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