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Items: 7

2.

Cytogenetic survey in couples with recurrent fetal wastage.

Fryns JP, Kleczkowska A, KubieĊ„ E, Petit P, Van den Berghe H.

Hum Genet. 1984;65(4):336-54.

PMID:
6693122
3.

Balanced reciprocal translocations: risk factors for aneuploid segregant viability.

Davis JR, Rogers BB, Hagaman RM, Thies CA, Veomett IC.

Clin Genet. 1985 Jan;27(1):1-19. Review.

PMID:
3884190
4.
5.

Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18.

Wilson GN, Heller KB, Elterman RD, Schneider NR.

Am J Med Genet. 1990 Aug;36(4):506-10. Review.

PMID:
1697142
6.

Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype.

Fryns JP, Vinken L, Marien J, Van den Berghe H.

Hum Genet. 1979 Feb 15;46(3):341-4.

PMID:
437778
7.

Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Neu RL, Ortega CC, Barg GA, Pinto W Jr, Gardner LI, Howell WM, Denton TE.

J Med Genet. 1976 Dec;13(6):520-2.

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