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Results: 18

Related Articles by Review for PubMed (Select 3233775)

1.

Terminal deletion of the short arm of chromosome 5.

Baccichetti C, Lenzini E, Artifoni L, Caufin D, Marangoni P.

Clin Genet. 1988 Oct;34(4):219-23.

PMID:
3233775
2.

Phenotypic and phoniatric findings in mosaic cri du chat syndrome.

Romano C, Ragusa RM, Scillato F, Greco D, Amato G, Barletta C.

Am J Med Genet. 1991 Jun 15;39(4):391-5. Review.

PMID:
1877615
3.

Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat).

Levy B, Dunn TM, Kern JH, Hirschhorn K, Kardon NB.

Am J Med Genet. 2002 Mar 15;108(3):192-7. Review.

PMID:
11891684
4.

Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion of chromosome 5.

Ono K, Ohashi Y, Nakano H, Togashi H, Kannari Y, Isono S.

Jpn J Hum Genet. 1993 Sep;38(3):319-28. Review.

PMID:
8260723
5.

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Niebuhr E.

Hum Genet. 1978 Nov 16;44(3):227-75. Review.

PMID:
365706
6.

A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literature.

Iqbal MA, Ahmed MZ, Wu D, Sakati N.

Am J Med Genet. 1997 May 16;70(2):174-8. Review.

PMID:
9128939
7.

[The cat cry (cri du chat) syndrome: report of a case with review of 10 cases at the National Taiwan University Hospital].

Chuang SM, Wang TR, Jean HH, Lee FY.

Taiwan Yi Xue Hui Za Zhi. 1989 Jun;88(6):635-8, 628-9. Review. Chinese.

PMID:
2677233
8.

Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.

Azman BZ, Akhir SM, Zilfalil BA, Ankathil R.

Singapore Med J. 2008 Apr;49(4):e98-e100. Review.

9.

Terminal deletion of the long arm of chromosome 4 in a mother and two sons.

Descartes M, Keppler-Noreuil K, Knops J, Longshore JW, Finley WH, Carroll AJ.

Clin Genet. 1996 Dec;50(6):538-40. Review.

PMID:
9147894
10.

Delineation of 14q32.3 deletion syndrome.

Ortigas AP, Stein CK, Thomson LL, Hoo JJ.

J Med Genet. 1997 Jun;34(6):515-7. Review.

11.

A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridization.

Flaherty L, Moloney J, Watson N, Robson L, Bousfield L, Smith A.

J Intellect Disabil Res. 1998 Jun;42 ( Pt 3):254-8. Review.

PMID:
9678410
12.

De novo complete trisomy 5p: clinical report and FISH studies.

Reichenbach H, Holland H, Dalitz E, Demandt C, Meiner A, Chudoba I, Lemke J, Claussen U, Froster UG.

Am J Med Genet. 1999 Aug 27;85(5):447-51. Review.

PMID:
10405440
13.

Cri du Chat syndrome.

Cerruti Mainardi P.

Orphanet J Rare Dis. 2006 Sep 5;1:33. Review.

14.

[Prognosis in the cri-du-chat syndrome].

Oosterwijk JC, Verboom AJ, Bijlsma JB.

Tijdschr Kindergeneeskd. 1987 Dec;55(6):226-33. Review. Dutch.

PMID:
3327195
15.

Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.

Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H.

Am J Med Genet. 1995 Jan 16;55(2):147-54. Review.

PMID:
7717413
16.

Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3).

Cervera M, Sánchez S, Molina B, Alcántara MA, Del Castillo V, Carnevale A, González-del Angel A.

Am J Med Genet A. 2005 Aug 1;136A(4):381-5. Review.

PMID:
16001443
17.

The cri-du-chat syndrome with an apparently normal karyotype.

McGavin DD, Cant JS, Ferguson-Smith MA, Ellis PM.

Lancet. 1967 Aug 12;2(7511):326-30. Review. No abstract available.

PMID:
4143723
18.

[Recent research advances in 5q- syndrome].

Wang HQ, Sheng W, Shao ZH.

Zhonghua Xue Ye Xue Za Zhi. 2011 Oct;32(10):707-9. Review. Chinese. No abstract available.

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