✦ LIBER ✦
Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q
✍ Scribed by Terrett, Jonathan A.; Newbury-Ecob, Ruth; Cross, Gareth S.; Fenton, Iain; Raeburn, J. Alexander; Young, Ian D.; Brook, J. David
- Book ID
- 109915682
- Publisher
- Nature Publishing Group
- Year
- 1994
- Tongue
- English
- Weight
- 363 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1061-4036
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