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Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene--Deletion Syndrome
- Source :
- American Journal of Human Genetics. Nov, 2000, Vol. 67 Issue 5, 1327
- Publication Year :
- 2000
- Subjects :
- Genetic research -- Analysis
Human genetics -- Research
Biological sciences
Subjects
Details
- ISSN :
- 00029297
- Volume :
- 67
- Issue :
- 5
- Database :
- Gale General OneFile
- Journal :
- American Journal of Human Genetics
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.67582559