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Results: 1 to 20 of 27

1.

A patient with a ring chromosome 2 and microdeletion of 2q detected using FISH: Further support for "ring chromosome 2 syndrome".

Alkuraya FS, Kimonis VE, Holt L, Murata-Collins JL.

Am J Med Genet A. 2005 Feb 1;132(4):447-9. Review. No abstract available.

PMID:
15580637
[PubMed - indexed for MEDLINE]
2.

Opitz "C" trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q.

Czakó M, Riegel M, Morava E, Bajnóczky K, Kosztolányi G.

Am J Med Genet A. 2004 Dec 15;131(3):310-2.

PMID:
15540175
[PubMed - indexed for MEDLINE]
3.

A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH.

Dee SL, Clark AT, Willatt LR, Yates JR.

J Med Genet. 2001 Sep;38(9):E32. No abstract available.

PMID:
11546833
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Ring 2 chromosome: ten-year follow-up report.

Lacassie Y, Arriaza MI, Vargas A, La Motta I.

Am J Med Genet. 1999 Jul 16;85(2):117-22. Review.

PMID:
10406663
[PubMed - indexed for MEDLINE]
5.

Chromosomal aberrations in couples undergoing intracytoplasmic sperm injection: influence on implantation and ongoing pregnancy rates.

Scholtes MC, Behrend C, Dietzel-Dahmen J, van Hoogstraten DG, Marx K, Wohlers S, Verhoeven H, Zeilmaker GH.

Fertil Steril. 1998 Nov;70(5):933-7.

PMID:
9806579
[PubMed - indexed for MEDLINE]
6.

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

Horsley SW, Knight SJ, Nixon J, Huson S, Fitchett M, Boone RA, Hilton-Jones D, Flint J, Kearney L.

J Med Genet. 1998 Sep;35(9):722-6.

PMID:
9733029
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Inflammatory arthropathies in children with chromosomal abnormalities.

Ihnat DH, McIlvain-Simpson G, Conard K, Scott CI, Singsen BH.

J Rheumatol. 1993 Apr;20(4):742-6.

PMID:
8496877
[PubMed - indexed for MEDLINE]
8.

Ring chromosome 2 in a child with growth failure and few congenital abnormalities.

Vigfusson NV, Kapstafer KJ, Lloyd MA.

Am J Med Genet. 1980;7(3):383-9.

PMID:
7468662
[PubMed - indexed for MEDLINE]
9.

A malformed baby with two separate de novo translocations.

Chewings WE, Cocks TP, Gardner RJ, Clarkson JE.

J Med Genet. 1982 Feb;19(1):70-1. No abstract available.

PMID:
7069750
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.

Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR.

Am J Med Genet. 1982 Jan;11(1):61-75.

PMID:
7065004
[PubMed - indexed for MEDLINE]
11.

The cytogenetic and clinical implications of a ring chromosome 2.

Cote GB, Katsantoni A, Deligeorgis D.

Ann Genet. 1981;24(4):231-5.

PMID:
6977305
[PubMed - indexed for MEDLINE]
12.

Autosomal dominant anterior polar cataracts associated with a familial 2;14 translocation.

Moross T, Vaithilingam SS, Styles S, Gardner HA.

J Med Genet. 1984 Feb;21(1):52-3.

PMID:
6694185
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Cytogenetic survey in couples with recurrent fetal wastage.

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

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

PMID:
6693122
[PubMed - indexed for MEDLINE]
14.

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]
15.

Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case.

Subrt I, Kozák J, Hníková O.

Hum Hered. 1973 Apr;23(4):331-7. No abstract available.

PMID:
4130027
[PubMed - indexed for MEDLINE]
16.

The significance of pericentric inversions of chromosome 2.

Djalali M, Steinbach P, Bullerdiek J, Holmes-Siedle M, Verschraegen-Spae MR, Smith A.

Hum Genet. 1986 Jan;72(1):32-6.

PMID:
3943862
[PubMed - indexed for MEDLINE]
17.

Dup(3)(p2----pter) in two families, including one infant with cyclopia.

Gimelli G, Cuoco C, Lituania M, Cordone M, Aricò M, Bianchi E, Maraschio P, Zuffardi O.

Am J Med Genet. 1985 Feb;20(2):341-8.

PMID:
3919583
[PubMed - indexed for MEDLINE]
18.

On the significance of pericentric inversions of chromosome 2.

Wahlström J, Kyllerman M.

Hum Genet. 1986 Nov;74(3):328-9. No abstract available.

PMID:
3781564
[PubMed - indexed for MEDLINE]
19.

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]
20.

Abnormal chromosome complement resulting from a familial inversion of chromosome 2.

Richter S, Lockwood B, Lockwood D, Allanson J.

J Med Genet. 1989 Nov;26(11):725-9.

PMID:
2479747
[PubMed - indexed for MEDLINE]
Free PMC Article

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