Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome? (Q30718704)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome? |
scientific article |
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Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome? (English)
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Grosso S
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Farnetani MA
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Berardi R
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Vivarelli R
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Vanni M
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Morgese G
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Balestri P
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1 August 2002
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111
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182-186
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