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Results: 12

1.

Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.

Velinov M, Gu H, Genovese M, Duncan C, Warburton P, Brooks SS, Jenkins EC.

Ann Genet. 2004 Apr-Jun;47(2):199-205.

PMID:
15183754
[PubMed - indexed for MEDLINE]
2.

Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas.

Chang M, Tsuchiya K, Batchelor RH, Rabinovitch PS, Kulander BG, Haggitt RC, Burmer GC.

Am J Pathol. 1994 Jan;144(1):1-6.

PMID:
8291601
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Partial trisomy 8 mosaicism with 46,XX/46,XX-8,+dic(8).

Ray M, Hunter AG.

Ann Genet. 1980;23(2):100-2.

PMID:
6967279
[PubMed - indexed for MEDLINE]
4.

Segregation analysis in reciprocal translocation carriers.

Petrosky DL, Borgaonkar DS.

Am J Med Genet. 1984 Sep;19(1):137-59.

PMID:
6496566
[PubMed - indexed for MEDLINE]
5.

[Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)].

Pfeiffer RA, Lenard HG.

Klin Padiatr. 1973 May;185(3):187-91. German. No abstract available.

PMID:
4795572
[PubMed - indexed for MEDLINE]
6.

Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomes.

Breg WR, Alderdice PW, Miller DA, Miller OJ.

Nat New Biol. 1972 Mar 22;236(64):76-8. No abstract available.

PMID:
4502457
[PubMed - indexed for MEDLINE]
7.

Studying human chromosomes today.

German J.

Am Sci. 1970 Mar-Apr;58(2):182-201. Review. No abstract available.

PMID:
4244681
[PubMed - indexed for MEDLINE]
8.

Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.

del Solar C, Uchida IA.

J Pediatr. 1974 Apr;84(4):534-8. No abstract available.

PMID:
4134885
[PubMed - indexed for MEDLINE]
9.

Fragile X testing in a diagnostic cytogenetics laboratory.

Voullaire LE, Webb GC, Leversha M.

J Med Genet. 1989 Jul;26(7):439-42.

PMID:
2473208
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitution.

Orye E, Craen M.

Clin Genet. 1976 Mar;9(3):289-301.

PMID:
1261067
[PubMed - indexed for MEDLINE]
11.

Duplication-deficiency of the short arm of chromosome 8 following artificial insemination.

Weleber RG, Verma RS, Kimberling WJ, Fieger HG Jr, lubs HA.

Ann Genet. 1976 Dec;19(4):241-7.

PMID:
1087853
[PubMed - indexed for MEDLINE]
12.

Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.

Hamers AJ, van Kempen C.

J Med Genet. 1977 Dec;14(6):451-5.

PMID:
604497
[PubMed - indexed for MEDLINE]
Free PMC Article

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