Journal article
Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity.
- Abstract:
-
Brachydactyly type B (BDB), an autosomal dominant disorder, is the most severe of the brachydactylies and is characterized by hypoplasia or absence of the terminal portions of the index to little fingers, usually with absence of the nails. The thumbs may be of normal length but are often flattened and occasionally are bifid. The feet are similarly but less severely affected. We have performed a genomewide linkage analysis of three families with BDB, two English and one Portugese. The two Engl...
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- Publication status:
- Published
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- Publisher copy:
- 10.1086/302255
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Bibliographic Details
- Journal:
- American journal of human genetics
- Volume:
- 64
- Issue:
- 2
- Pages:
- 578-585
- Publication date:
- 1999-02-01
- DOI:
- EISSN:
-
1537-6605
- ISSN:
-
0002-9297
- Source identifiers:
-
107638
Item Description
- Language:
- English
- Keywords:
- Pubs id:
-
pubs:107638
- UUID:
-
uuid:19462b5c-ba4a-4625-98be-72616c59ac44
- Local pid:
- pubs:107638
- Deposit date:
- 2013-11-16
Terms of use
- Copyright date:
- 1999
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