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Items: 6

1.

Prenatal diagnosis and characterization of an analphoid marker chromosome 16.

Tabet AC, Gosset P, Elghezal H, Fontaine S, Martinovic J, Encha Razavi F, Romana S, Vekemans M, Morichon-Delvallez N.

Prenat Diagn. 2004 Sep;24(9):733-6.

PMID:
15386469
2.

PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16 (16qh-).

Colls P, Sandalinas M, Pagidas K, Munné S.

Prenat Diagn. 2004 Sep;24(9):741-4.

PMID:
15386466
3.

Inverted duplication involving alpha satellite DNA resulting in a C-negative-band in the qh region of chromosome 16.

Jalal SM, Law ME, Dewald GW.

Am J Med Genet. 1993 May 15;46(3):351-2. No abstract available.

PMID:
8488887
4.

Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.

Eriksson B, Fraccaro M, Hultén M, Lindsten J, Thorén C, Tiepolo L.

Ann Genet. 1971 Dec;14(4):281-90. No abstract available.

PMID:
5316133
5.

Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Mikelsaar AV, Tüür SJ, Käosaar ME.

Humangenetik. 1973;20(2):89-101. No abstract available.

PMID:
4785172
6.

A Japanese case with an unusual variant of chromosome 16 with an extra C-negative, G-dark segment in the short arm.

Arinami T, Kondo I.

Jinrui Idengaku Zasshi. 1988 Sep;33(3):373-6. No abstract available.

PMID:
3204690

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