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Items: 13

1.
2.

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.

Babovic-Vuksanovic D, Jenkins SC, Ensenauer R, Newman DC, Jalal SM.

Am J Med Genet A. 2004 Jan 30;124A(3):318-22.

PMID:
14708108
3.

First familial case of ring chromosome 18 and monosomy 18 mosaicism.

Yardin C, Esclaire F, Terro F, Baclet MC, Barthe D, Laroche C.

Am J Med Genet. 2001 Dec 1;104(3):257-9. No abstract available.

PMID:
11754054
4.

Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis.

Rigola MA, Plaja A, Mediano C, Miró R, Egozcue J, Fuster C.

Am J Med Genet. 2001 Nov 15;104(1):37-41.

PMID:
11746025
5.

Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly.

de Pater JM, Scheres JM, Brons J.

Prenat Diagn. 1997 Sep;17(9):887-8. No abstract available.

PMID:
9316141
6.
7.

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome.

Mattei MG, Philip N, Passage E, Moisan JP, Mandel JL, Mattei JF.

Hum Genet. 1985;69(3):268-71.

PMID:
3980018
8.

Morphology alone does not make an isochromosome.

Schmutz SM, Pinno E.

Hum Genet. 1986 Mar;72(3):253-5.

PMID:
3957349
9.

Ring chromosome 18 in a mother and son.

Donlan MA, Dolan CR.

Am J Med Genet. 1986 May;24(1):171-4.

PMID:
3706404
10.

Ring 18 chromosome with mental retardation, hemidysmorphism, and mitochondrial encephalomyopathy.

Amit R, Gutman A, Udassin R, Barash V, Kohn G.

Pediatr Neurol. 1988 Sep-Oct;4(5):301-4.

PMID:
3242534
12.

Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype.

Williams CA, Frias JL, McCormick MK, Antonarakis SE, Cantu ES.

Am J Med Genet Suppl. 1990;7:110-4.

PMID:
2149936
13.

Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.

Fryns JP, Kleczkowska A, Smeets E, Van Den Berghe H.

Ann Genet. 1992;35(2):121-3.

PMID:
1524410

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