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January 1, 1992American Journal of Medical Genetics

Alagille syndrome with de Novo del(20) (p 11.2)

Ahmad S. Teebi Dodderi S. Krishna Murthy Eman Abdel Rahman Ismail A. A. Redha

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Abstract

We report on an Arab boy with Alagille syndrome and a de novo deletion of the short arm of chromosome 20 with a 46,XY, del(20)(p11.2) chromosome constitution. Other reported cases are briefly reviewed.

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Cite This Study

Teebi et al. (1992) studied this question.

synapsesocial.com/papers/6a93a2e21eecaf8548721066 https://doi.org/10.1002/ajmg.1320420109

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Alagille syndrome and deletion of 20p.Original Research · 1990 · 96 citations
2Del(20p) with manifestations of arteriohepatic dysplasiaOriginal Research · 1986 · 88 citations
3Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)Original Research · 1990 · 38 citations
4Arteriohepatic dysplasia: phenotypic features and family studiesOriginal Research · 1984 · 43 citations
5Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver diseaseOriginal Research · 1973 · 260 citations

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