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Results: 15

1.

Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms.

Lespinasse J, Gimelli S, Béna F, Antonarakis SE, Ansermet F, Paoloni-Giacobino A.

Eur J Med Genet. 2009 Jan-Feb;52(1):49-52. doi: 10.1016/j.ejmg.2008.10.001. Epub 2008 Oct 21.

PMID:
18992376
[PubMed - indexed for MEDLINE]
2.

Prenatal detection of deletion 6q13q15 in a complex karyotype.

Yu M, Obringer AC, Fowler MH, Hummel M, Wenger SL.

Prenat Diagn. 2005 Dec;25(12):1084-7. Review.

PMID:
16231325
[PubMed - indexed for MEDLINE]
3.

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.

Shaw-Smith C, Redon R, Rickman L, Rio M, Willatt L, Fiegler H, Firth H, Sanlaville D, Winter R, Colleaux L, Bobrow M, Carter NP.

J Med Genet. 2004 Apr;41(4):241-8.

PMID:
15060094
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Twenty-nail dystrophy in a mother and her 7-year-old daughter associated with balanced translocation 46, XX, t(6q13;10p13).

Balci S, Kanra G, Aypar E, Son YA.

Clin Dysmorphol. 2002 Jul;11(3):171-3.

PMID:
12072794
[PubMed - indexed for MEDLINE]
5.

Severe aplastic anaemia in association with a unique constitutional translocation 46,XY,t(6;10)(q13;q22)c.

Hudson J, Chown S, Lawler M, Duggan C, Temperley IJ, Secker-Walker L.

Br J Haematol. 1997 Dec;99(3):520-1.

PMID:
9401059
[PubMed - indexed for MEDLINE]
6.

Proximal interstitial 6q deletion: a recognizable syndrome.

Kumar R, Riordan D, Dawson AJ, Chudley AE.

Am J Med Genet. 1997 Aug 22;71(3):353-6. Review.

PMID:
9268108
[PubMed - indexed for MEDLINE]
7.

New insights into the phenotypes of 6q deletions.

Hopkin RJ, Schorry E, Bofinger M, Milatovich A, Stern HJ, Jayne C, Saal HM.

Am J Med Genet. 1997 Jun 27;70(4):377-86. Review.

PMID:
9182778
[PubMed - indexed for MEDLINE]
8.

Chromosomal studies of children with developmental language retardation.

Friedrich U, Dalby M, Staehelin-Jensen T, Bruun-Petersen G.

Dev Med Child Neurol. 1982 Oct;24(5):645-52. No abstract available.

PMID:
7141121
[PubMed - indexed for MEDLINE]
9.

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

Boué A, Gallano P.

Prenat Diagn. 1984 Spring;4 Spec No:45-67.

PMID:
6463033
[PubMed - indexed for MEDLINE]
10.

Deletions of the long arm of chromosome 6: two new cases and review of the literature.

Young RS, Fidone GS, Reider-Garcia PA, Hansen KL, McCombs JL, Moore CM.

Am J Med Genet. 1985 Jan;20(1):21-9. Review.

PMID:
3881954
[PubMed - indexed for MEDLINE]
11.

Deletion of proximal 6q: a clinical report and review of the literature.

Yamamoto Y, Okamoto N, Shiraishi H, Yanagisawa M, Kamoshita S.

Am J Med Genet. 1986 Nov;25(3):467-71.

PMID:
3789009
[PubMed - indexed for MEDLINE]
12.

Cytogenetic analysis of 688 couples experiencing multiple spontaneous abortions.

Castle D, Bernstein R.

Am J Med Genet. 1988 Mar;29(3):549-56.

PMID:
3376998
[PubMed - indexed for MEDLINE]
13.

The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Lindenbaum RH, Hultén M, McDermott A, Seabright M.

J Med Genet. 1985 Feb;22(1):24-8.

PMID:
3156995
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

De novo balanced reciprocal translocation 46,XY,t(6;8)(q13;q22).

Fried K, Rosenblatt M, Mundel G.

J Med Genet. 1977 Apr;14(2):142-4.

PMID:
853320
[PubMed - indexed for MEDLINE]
Free PMC Article

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