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Late manifestation of Indian childhood cirrhosis in a 3-year-old German girl

✍ Scribed by R. Trollmann; D. Neureiter; T. Lang; H. G. Dörr; R. Behrens


Publisher
Springer
Year
1999
Tongue
English
Weight
285 KB
Volume
158
Category
Article
ISSN
0340-6997

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A 3-year-old girl has a de novo deletion of 11q21-22.3. The patient was studied because of minor anomalies, disproportionate short stature, and developmental delay. The deletion was first detected by conventional cytogenetic analysis and defined further by using chromosome 11-specific YAC clones by