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Results: 9

1.

Centric fission of chromosome 9 in a boy with trisomy 9p.

Concolino D, Cinti R, Moricca M, Andria G, Strisciuglio P.

Am J Med Genet. 1998 Aug 27;79(1):35-7.

PMID:
9738866
[PubMed - indexed for MEDLINE]
2.

Delineation of supernumerary marker chromosomes in 38 patients.

Viersbach R, Engels H, Gamerdinger U, Hansmann M.

Am J Med Genet. 1998 Apr 1;76(4):351-8.

PMID:
9545101
[PubMed - indexed for MEDLINE]
3.

Evidence of chromosome 9 origin of the euchromatic variant band within 9qh.

Hoo JJ, Szego K, Wong P, Roland B.

Clin Genet. 1993 Jun;43(6):309-11.

PMID:
8370151
[PubMed - indexed for MEDLINE]
4.

Molecular cytogenetic characterization of two types of chromosome 9 variants.

Wang JC, Miller WA.

Cytogenet Cell Genet. 1994;67(3):190-2.

PMID:
8062595
[PubMed - indexed for MEDLINE]
5.

Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

Podruch PE, Weisskopf B.

J Pediatr. 1974 Jul;85(1):92-5. No abstract available.

PMID:
4855265
[PubMed - indexed for MEDLINE]
6.

A chromosomal break and partial deletion of a number 9 chromosome.

Smith GF, Sachdeva S, Justice P.

Hum Hered. 1973;23(6):561-7. No abstract available.

PMID:
4792221
[PubMed - indexed for MEDLINE]
7.

Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques.

Evans HJ, Buckton KE, Sumner AT.

Chromosoma. 1971;35(3):310-25. No abstract available.

PMID:
4109086
[PubMed - indexed for MEDLINE]
8.

Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.

Shapiro SD, Hansen KL, Littlefield CA.

Am J Med Genet. 1985 Feb;20(2):271-6.

PMID:
3976720
[PubMed - indexed for MEDLINE]
9.

Identification of a break-prone structure in the 9q1 heterochromatic region.

Mamuris Z, Aurias A, Dutrillaux B.

Hum Genet. 1991 Jan;86(3):261-4.

PMID:
1997378
[PubMed - indexed for MEDLINE]

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