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Results: 6

1.

Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements.

Simopoulou M, Harper JC, Fragouli E, Mantzouratou A, Speyer BE, Serhal P, Ranieri DM, Doshi A, Henderson J, Rodeck CH, Delhanty JD.

Prenat Diagn. 2003 Aug;23(8):652-62.

PMID:
12913872
[PubMed - indexed for MEDLINE]
2.

Distal 5q deletion syndrome: phenotypic correlations.

Schafer IA, Robin NH, Posch JJ, Clark BA, Izumo S, Schwartz S.

Am J Med Genet. 2001 Sep 15;103(1):63-8. Review.

PMID:
11562936
[PubMed - indexed for MEDLINE]
3.

Chromosome specific comparative genome hybridisation for determining the origin of intrachromosomal duplications.

Griffin DK, Sanoudou D, Adamski E, McGiffert C, O'Brien P, Wienberg J, Ferguson-Smith MA.

J Med Genet. 1998 Jan;35(1):37-41.

PMID:
9475092
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

Daniel A, Hook EB, Wulf G.

Am J Med Genet. 1989 May;33(1):14-53.

PMID:
2750783
[PubMed - indexed for MEDLINE]
6.

Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndrome.

Curry CJ, Loughman WD, Francke U, Hall BD, Golbus MS, Derstine J, Epstein CJ.

Clin Genet. 1979 May;15(5):454-61.

PMID:
445868
[PubMed - indexed for MEDLINE]

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