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1
Genetic markers on chromosome 7.
J Med Genet. 1988 May;25(5):294-306. doi: 10.1136/jmg.25.5.294.
2
Molecular genetics of human chromosome 4.
J Med Genet. 1986 Jun;23(3):193-9. doi: 10.1136/jmg.23.3.193.
3
Chromosome 1 in relation to human disease.
J Med Genet. 1986 Apr;23(2):107-15. doi: 10.1136/jmg.23.2.107.
4
The morbid anatomy of the human genome: a review of gene mapping in clinical medicine. 4.
Medicine (Baltimore). 1988 Jan;67(1):1-19. doi: 10.1097/00005792-198801000-00001.
5
Genetic linkage map of human chromosome 7 with 63 DNA markers.
Proc Natl Acad Sci U S A. 1987 Nov;84(22):8006-10. doi: 10.1073/pnas.84.22.8006.
6
Chromosome 7.
Genet Test. 2002 Summer;6(2):141-61. doi: 10.1089/10906570260199429.
7
Mapping the human genome, cloned genes, DNA polymorphisms, and inherited disease.
Adv Hum Genet. 1982;12:341-452. doi: 10.1007/978-1-4615-8315-8_5.
8
Toward the complete genomic map and molecular pathology of human chromosome 4.
Hum Genet. 1994 Jul;94(1):1-18. doi: 10.1007/BF02272834.
9
Construction of linkage maps with DNA markers for human chromosomes.
Nature. 1985;313(5998):101-5. doi: 10.1038/313101a0.

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1
The mapping of human chromosomes.
Annu Rev Genet. 1971;5:81-120. doi: 10.1146/annurev.ge.05.120171.000501.
3
Chromosome 7 in ataxia-telangiectasia.
J Pediatr. 1980 Sep;97(3):440-1. doi: 10.1016/s0022-3476(80)80200-9.
4
Interstitial deletion of the long arm of chromosome 7.
Hum Genet. 1980;54(1):19-23. doi: 10.1007/BF00279044.
5
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia.
Mutat Res. 1980 Feb;69(2):369-74. doi: 10.1016/0027-5107(80)90101-3.
6
A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling.
Prenat Diagn. 1981 Jan;1(1):81-4. doi: 10.1002/pd.1970010113.
7
Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia.
Cancer Genet Cytogenet. 1981 Nov;4(3):197-214. doi: 10.1016/0165-4608(81)90014-5.
8
Interstitial deletion of the short arm of chromosome 7 without craniosynostosis.
Clin Genet. 1981 Jun;19(6):456-61. doi: 10.1111/j.1399-0004.1981.tb02064.x.

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