Cornelia de lange syndrome. Report of 2 cases in siblings.

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作者信息

Ingle V N, Mali V B

出版信息

Indian J Pediatr. 1970 Apr;37(267):149-51. doi: 10.1007/BF02750907.

DOI:10.1007/BF02750907

PMID:5473636

Abstract

摘要

相似文献

Cornelia de lange syndrome. Report of 2 cases in siblings.

Indian J Pediatr. 1970 Apr;37(267):149-51. doi: 10.1007/BF02750907.

Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: case report.

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本文引用的文献

THE DE LANGE SYNDROME.

Am J Dis Child. 1965 Apr;109:325-32. doi: 10.1001/archpedi.1965.02090020327012.

BRACHMANN/DE LANGE SYNDROME.

Lancet. 1964 Nov 7;2(7367):1019. doi: 10.1016/s0140-6736(64)90980-8.

THE CORNELIA DE LANGE SYNDROME.

J Pediatr. 1963 Nov;63:1000-20. doi: 10.1016/s0022-3476(63)80234-6.

TYPUS DEGENERATIVUS AMSTELODAMENSIS.

Arch Dis Child. 1963 Aug;38(200):349-57. doi: 10.1136/adc.38.200.349.

Familial de Lange syndrome with chromosome abnormalities.

Pediatrics. 1966 Jan;37(1):92-101.

The Cornelia de Lange syndrome: clinical and cytogenetic interpretations.

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

Pathological features in the de Lange syndrome.

Acta Paediatr Scand. 1969 Sep;58(5):470-80. doi: 10.1111/j.1651-2227.1969.tb04748.x.

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相似文献

Cornelia de lange syndrome. Report of 2 cases in siblings.

Indian J Pediatr. 1970 Apr;37(267):149-51. doi: 10.1007/BF02750907.

Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: case report.

BMC Cancer. 2016 Jun 13;16:365. doi: 10.1186/s12885-016-2402-2.

Otolaryngological presentations of Cornelia de Lange syndrome.

Int J Pediatr Otorhinolaryngol. 2014 Sep;78(9):1548-50. doi: 10.1016/j.ijporl.2014.05.032. Epub 2014 Jun 19.

Chromosomes in the Cornelia de Lange syndrome.

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

[A case of Cornelia de Lange syndrome with retentio testis].

Hinyokika Kiyo. 1985 Jul;31(7):1203-10.

Epileptic features in Cornelia de Lange syndrome: case report and literature review.

Brain Dev. 2014 Nov;36(10):837-43. doi: 10.1016/j.braindev.2013.12.008. Epub 2014 Jan 22.

[Cornelia de Lange syndrome and the woman behind the syndrome].

Tidsskr Nor Laegeforen. 1995 Dec 10;115(30):3724-6.

Cornelia de Lange syndrome in an Egyptian child.

Birth Defects Orig Artic Ser. 1975;11(2):362-3.

A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findings.

Singapore Med J. 2006 Aug;47(8):724-7.

Behavioural phenotype of Cornelia de Lange syndrome: case-control study.

Br J Psychiatry. 2008 Dec;193(6):466-70. doi: 10.1192/bjp.bp.107.044370.

本文引用的文献

THE DE LANGE SYNDROME.

Am J Dis Child. 1965 Apr;109:325-32. doi: 10.1001/archpedi.1965.02090020327012.

BRACHMANN/DE LANGE SYNDROME.

Lancet. 1964 Nov 7;2(7367):1019. doi: 10.1016/s0140-6736(64)90980-8.

THE CORNELIA DE LANGE SYNDROME.

J Pediatr. 1963 Nov;63:1000-20. doi: 10.1016/s0022-3476(63)80234-6.

TYPUS DEGENERATIVUS AMSTELODAMENSIS.

Arch Dis Child. 1963 Aug;38(200):349-57. doi: 10.1136/adc.38.200.349.

Familial de Lange syndrome with chromosome abnormalities.

Pediatrics. 1966 Jan;37(1):92-101.

The Cornelia de Lange syndrome: clinical and cytogenetic interpretations.

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

Pathological features in the de Lange syndrome.

Acta Paediatr Scand. 1969 Sep;58(5):470-80. doi: 10.1111/j.1651-2227.1969.tb04748.x.