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Items: 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
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.

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
4.

Segregation analysis in reciprocal translocation carriers.

Petrosky DL, Borgaonkar DS.

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

PMID:
6496566
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
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
7.

Studying human chromosomes today.

German J.

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

PMID:
4244681
8.
9.

Fragile X testing in a diagnostic cytogenetics laboratory.

Voullaire LE, Webb GC, Leversha M.

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

10.
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
12.

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