A novel locus for parietal foramina maps to chromosome 4q21-q23
- 7 August 2003
- journal article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 48 (8) , 420-424
- https://doi.org/10.1007/s10038-003-0050-2
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion SyndromeAmerican Journal of Human Genetics, 2000
- Haploinsufficiency ofALX4as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion SyndromeAmerican Journal of Human Genetics, 2000
- A Locus for Brachydactyly Type A-1 Maps to Chromosome 2q35-q36American Journal of Human Genetics, 2000
- Interstitial deletion of 11 (P11.2p12): A newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2)American Journal of Medical Genetics, 1996
- Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardationAmerican Journal of Medical Genetics, 1993
- A Procedure for Combining Two-Point Lod Scores into a Summary Multipoint MapHuman Heredity, 1993
- Hereditary cranium bifidum and symmetric parietal foramina are the same entityAmerican Journal of Medical Genetics, 1990
- Parietal foramina in the Saethre-Chotzen syndrome.Journal of Medical Genetics, 1985
- Symptomatic Large Parietal ForaminaNeurosurgery, 1982
- Evolution and significance of giant parietal foraminaJournal of Neurosurgery, 1972