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Items: 17

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.

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.

8.

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
9.

Delineation of 14q32.3 deletion syndrome.

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

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

10.

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
11.

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
12.

[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
13.

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
14.

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
15.

Cri du Chat syndrome.

Cerruti Mainardi P.

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

16.

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
17.

[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.

PMID:
22339837
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