FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly (Q37130034)
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scientific article published on 28 June 2013
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly |
scientific article published on 28 June 2013 |
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FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly (English)
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Catheline Vilain
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Guy Van Vliet
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Nicolas Simonis
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Nelle Lambert
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Camille Perazzolo
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Deepthi C de Silva
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Boyan Dimitrov
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Claudine Heinrichs
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Sandra Janssens
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Bronwyn Kerr
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Philippe Lepage
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Georges Casimir
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Marc Abramowicz
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