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Results: 1 to 20 of 57

1.

Antenatal diagnosis of deletion chromosome 11(q23-qter) (Jacobsen syndrome).

Foley P, McAuliffe F, Mullarkey M, Reardon W.

Clin Dysmorphol. 2007 Jul;16(3):177-9.

PMID:
17551332
[PubMed - indexed for MEDLINE]
2.

Congenital diaphragmatic hernia associated with duplication of 11q23-qter.

Klaassens M, Scott DA, van Dooren M, Hochstenbach R, Eussen HJ, Cai WW, Galjaard RJ, Wouters C, Poot M, Laudy J, Lee B, Tibboel D, de Klein A.

Am J Med Genet A. 2006 Jul 15;140(14):1580-6.

PMID:
16770801
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C.

J Med Genet. 2001 Nov;38(11):740-4.

PMID:
11694545
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts.

Chen CP, Chern SR, Tzen CY, Lee MS, Pan CW, Chang TY, Wang W.

Prenat Diagn. 2001 Apr;21(4):317-20.

PMID:
11288126
[PubMed - indexed for MEDLINE]
5.
6.

The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination.

Hill AS, Foot NJ, Chaplin TL, Young BD.

Hum Mol Genet. 2000 Jun 12;9(10):1525-32.

PMID:
10888603
[PubMed - indexed for MEDLINE]
Free Article
7.

Ebstein anomaly associated with rearrangements of chromosomal region 11q.

de Lonlay-Debeney P, de Blois MC, Bonnet D, Amiel J, Abadie V, Picq M, Lyonnet S, Sidi D, Munnich A, Vekemans M, Cormier-Daire V.

Am J Med Genet. 1998 Nov 2;80(2):157-9.

PMID:
9805133
[PubMed - indexed for MEDLINE]
8.

Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.

Petković I, de Capoa A, Giancotti P, Barisić I.

Clin Genet. 1996 Dec;50(6):515-9.

PMID:
9147886
[PubMed - indexed for MEDLINE]
9.

At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Smeets D, van Ravenswaaij C, de Pater J, Gerssen-Schoorl K, Van Hemel J, Janssen G, Smits A.

J Med Genet. 1997 Jan;34(1):18-23.

PMID:
9032644
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.

Chen CP, Liu FF, Jan SW, Yang YC, Lan CC.

Prenat Diagn. 1996 Dec;16(12):1137-40.

PMID:
8994250
[PubMed - indexed for MEDLINE]
11.

Risk estimates for balanced reciprocal translocation carriers--prenatal diagnosis experience.

Barisić I, Zergollern L, Muzinić D, Hitrec V.

Clin Genet. 1996 Mar;49(3):145-51.

PMID:
8737980
[PubMed - indexed for MEDLINE]
12.

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid.

Soler A, Carrio A, Perez-Vidal MT, Borrell A, Fortuny A.

Prenat Diagn. 1993 Feb;13(2):137-41.

PMID:
8464833
[PubMed - indexed for MEDLINE]
13.

Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22).

Slater HR, Voullaire LE, Vaux CE, Bankier A, Pertile M, Choo KH.

Am J Med Genet. 1993 Jun 1;46(4):434-7.

PMID:
8357017
[PubMed - indexed for MEDLINE]
14.

Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.

Sullivan BA, Leana-Cox J, Schwartz S.

Am J Med Genet. 1993 Aug 15;47(2):223-30.

PMID:
8213910
[PubMed - indexed for MEDLINE]
15.

Monosomy 11q: report of two familial cases and review of the literature.

Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L.

Am J Med Genet. 1993 Sep 1;47(3):312-7. Review.

PMID:
8135272
[PubMed - indexed for MEDLINE]
16.

Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.

Koiffmann CP, Gonzalez CH, Vianna-Morgante AM, Kim CA, Odone-Filho V, Wajntal A.

Am J Med Genet. 1995 Jul 31;58(1):46-9. Review.

PMID:
7573155
[PubMed - indexed for MEDLINE]
17.

Central nervous system abnormalities in chromosome deletion at 11q23.

Ono J, Harada K, Hasegawa T, Sakurai K, Kodaka R, Tanabe Y, Tanaka J, Igarashi T, Nagai T, Okada S.

Clin Genet. 1994 Jun;45(6):325-9.

PMID:
7523004
[PubMed - indexed for MEDLINE]
18.

[Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author's transl)].

Pangalos C, Couturier J, Bartsocas C, Theodorou S.

Nouv Presse Med. 1980 Nov 1;9(41):3065-7. French.

PMID:
7443445
[PubMed - indexed for MEDLINE]
19.

Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

Schinzel A, Schmid W, Auf der Maur P, Moser H, Degenhardt KH, Geisler M, Grubisic A.

Hum Genet. 1981;56(3):249-62.

PMID:
7239508
[PubMed - indexed for MEDLINE]
20.

Duplication of distal 11q and 22p occurrence in two unrelated families.

Najafzadeh TM, Dumars KW.

Am J Med Genet. 1981;8(3):341-7.

PMID:
7234904
[PubMed - indexed for MEDLINE]

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