Chromosome banding study of the Cornelia De Lange syndrome.

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A de novo t (X;8)(p11.2;q24.3) demonstrating Cornelia de Lange syndrome phenotype.

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Fetus with interstitial del(5)(p13.1p14.2) diagnosed postnatally with Cornelia de Lange syndrome.

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Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.

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Chromosomal anomaly associated with Cornelia de Lange's syndrome.

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[Chromosome abnormalities in a case of Cornelia De Lange syndrome (typus degenerativus amstedolamensis)].

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Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome.

Am J Med Genet. 2001 Jun 15;101(2):120-9.

2

Chromosomes in the Cornelia de Lange syndrome.

Hum Genet. 1981;59(4):271-6. doi: 10.1007/BF00295457.

本文引用的文献

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TRANSLOCATION IN DE LANGE'S SYNDROME?

Lancet. 1965 Aug 28;2(7409):445-6. doi: 10.1016/s0140-6736(65)90803-2.

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De Lange syndrome: report of 20 cases.

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Familial de Lange syndrome with chromosome abnormalities.

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Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl.

Stain Technol. 1965 Nov;40(6):333-8. doi: 10.3109/10520296509116440.

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The Cornelia de Lange syndrome--a case report with mild mental retardation.

Am J Ment Defic. 1965 Nov;70(3):438-42.

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The Cornelia de Lange syndrome: clinical and cytogenetic interpretations.

Can Med Assoc J. 1965 Sep 11;93(11):577-86.

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An inherited chromosome aberration in a girl with signs of de Lange syndrome.

Acta Paediatr Scand. 1968 Nov;57(6):547-52. doi: 10.1111/j.1651-2227.1968.tb06978.x.

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De Lange's Amsterdam dwarfism: case report and etiological considerations.

Am J Ment Defic. 1967 May;71(6):994-1003.

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Chromosomal anomaly associated with Cornelia de Lange's syndrome.

Acta Paediatr Acad Sci Hung. 1972;13(1):51-5.

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A rapid banding technique for human chromosomes.

Lancet. 1971 Oct 30;2(7731):971-2. doi: 10.1016/s0140-6736(71)90287-x.

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