Publication
| White RA, Dowler LL, Angeloni SV, Pasztor LM, MacArthur CA, Assignment of FGF8 to human chromosome 10q25-q26: mutations in FGF8 may be responsible for some types of acrocephalosyndactyly linked to this region. Genomics30:109-11 1995 |
| PubMed ID: 8595889 |
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| Records Return:
(1)
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| Catalog ID | Description | Collection_Type_id |
| MBP0002 | NIGMS HUMAN/RODENT SOMATIC CELL HYBRID MAPPING PANEL #2 DNA | |
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