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Results: 11

1.

Prenatal detection of rare chromosomal autosomal abnormalities in Europe.

Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballin MR, Guitart M; EUROSCAN Working Group.

Am J Med Genet A. 2003 May 1;118A(4):319-27.

PMID:
12687662
[PubMed - indexed for MEDLINE]
2.

Prenatal diagnosis of mosaic tetrasomy 10p associated with megacisterna magna, echogenic focus of left ventricle, umbilical cord cysts and distal arthrogryposis.

Wu YC, Yu MT, Chen LC, Chen CL, Yang ML.

Am J Med Genet A. 2003 Mar 15;117A(3):278-81.

PMID:
12599193
[PubMed - indexed for MEDLINE]
3.

Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case.

Granata P, Mazzola D, Righi R, Minelli E, Salvatoni A, Baroli P, Maggi F, Casalone R.

Ann Genet. 2000 Jan-Mar;43(1):45-50. Review.

PMID:
10818221
[PubMed - indexed for MEDLINE]
4.

Pure trisomy 10p involving an isochromosome 10p.

Berend SA, Shaffer LG, Bejjani BA.

Clin Genet. 1999 May;55(5):367-71.

PMID:
10422809
[PubMed - indexed for MEDLINE]
5.

Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis.

Stone D, Ning Y, Guan XY, Kaiser-Kupfer M, Wynshaw-Boris A, Biesecker L.

Hum Genet. 1996 Oct;98(4):396-402.

PMID:
8792811
[PubMed - indexed for MEDLINE]
6.

A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia.

Calabrese G, Franchi PG, Stuppia L, Mingarelli R, Rossi C, Ramenghi L, Marino M, Morizio E, Peila R, Antonucci A, et al.

J Med Genet. 1994 Oct;31(10):804-6.

PMID:
7837258
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Congenital glaucoma associated with a chromosomal defect. A histologic study.

Broughton WL, Fine BS, Zimmerman LE.

Arch Ophthalmol. 1981 Mar;99(3):481-6.

PMID:
7213170
[PubMed - indexed for MEDLINE]
8.

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]
9.

C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations.

Elliott D, Thomas GH, Condron CJ, Khuri N, Richardson F.

Am J Dis Child. 1970 Jan;119(1):72-3. No abstract available.

PMID:
5410297
[PubMed - indexed for MEDLINE]
10.

Physical retardation is associated with ring chromosome mosaicism: 46, XX,r(10)/45, XX,10 minus.

Lansky S, Daniel W, Fleiszar K.

J Med Genet. 1977 Feb;14(1):61-3.

PMID:
839503
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Four families with immunodeficiency and chromosome abnormalities.

Candy DC, Hayward AR, Hughes DT, Layward L, Soothill JF.

Arch Dis Child. 1979 Jul;54(7):518-23.

PMID:
314782
[PubMed - indexed for MEDLINE]
Free PMC Article

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