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Items: 1 to 20 of 26

1.

Azoospermia in a man with a constitutional ring 22 chromosome.

Zuccarello D, Dallapiccola B, Novelli A, Foresta C.

Eur J Med Genet. 2010 Nov-Dec;53(6):389-91. doi: 10.1016/j.ejmg.2010.07.014. Epub 2010 Aug 10.

PMID:
20709628
2.

Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.

Hastings RJ, Nisbet DL, Waters K, Spencer T, Chitty LS.

Prenat Diagn. 1999 May;19(5):436-45. Review.

PMID:
10360512
3.

Delineation of supernumerary marker chromosomes in 38 patients.

Viersbach R, Engels H, Gamerdinger U, Hansmann M.

Am J Med Genet. 1998 Apr 1;76(4):351-8.

PMID:
9545101
4.

Maternal uniparental disomy 22 has no impact on the phenotype.

Schinzel AA, Basaran S, Bernasconi F, Karaman B, Yüksel-Apak M, Robinson WP.

Am J Hum Genet. 1994 Jan;54(1):21-4.

5.

Complex chromosomal rearrangement leading to partial trisomy 22.

Hansteen IL, Schirmer L, Hestetun S, Brøgger A.

J Med Genet. 1980 Feb;17(1):66-8.

6.

Chromosome abnormalities in 150 couples with multiple spontaneous abortions.

Husslein P, Huber J, Wagenbichler P, Schnedl W.

Fertil Steril. 1982 Mar;37(3):379-83.

PMID:
7199485
8.

Oligospermia and infertility in a man with varicocele and G chromosome translocation.

Hasen J, Bartalos M.

J Urol. 1974 Jan;111(1):85-7. No abstract available.

PMID:
4813560
9.

Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Mikelsaar AV, Tüür SJ, Käosaar ME.

Humangenetik. 1973;20(2):89-101. No abstract available.

PMID:
4785172
10.

Monozygotic twins with ring chromosome 22.

Lindenbaum RH, Bobrow M, Barber L.

J Med Genet. 1973 Mar;10(1):85-9. No abstract available.

11.

Dicentric Ph1 chromosome.

Whang-Peng J, Knutsen TA, Lee EC.

J Natl Cancer Inst. 1973 Dec;51(6):2009-12. No abstract available.

PMID:
4520100
12.

Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

Warren RJ, Rimoin DL, Summitt RL.

Am J Hum Genet. 1973 Jan;25(1):77-81. No abstract available.

13.
14.

Frequency of deletion of short arm satellites in acrocentric chromosomes.

Nielsen J, Friedrich U, Hreidarsson AB.

J Med Genet. 1974 Jun;11(2):177-80. No abstract available.

15.

Letter: Brilliantly fluorescing enlarged short arms D or G.

Nielsen J, Friedrich U, Hreidarsson AB, Noel B, Quack B, Mottet J.

Lancet. 1974 May 25;1(7865):1049-50. No abstract available.

PMID:
4133722
16.
17.

Ring chromosome 22: a case report.

Severien C, Felix S, Bartholomé K.

Klin Padiatr. 1991 Nov-Dec;203(6):467-9.

PMID:
1721941
18.

A case of "g 2 deletion syndrome": ring or partial monosomy? (46,XX,22r or 46,XX,22p- ?).

Milani-Comparetti M, Rossolini V, Pace DP, Burroni M, Magistrelli R, Saccucci F.

Acta Genet Med Gemellol (Roma). 1975;24(3-4):311-3.

PMID:
1235937
19.

A case of ring chromosome.

Brookfield DS, Walker S.

J Med Genet. 1976 Dec;13(6):530-2.

20.

Phenotypic correlations in patients with ring chromosome 22.

Hunter AG, Ray M, Wang HS, Thompson DR.

Clin Genet. 1977 Oct;12(4):239-49.

PMID:
912941

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