| scholarly article | Q13442814 |
| P50 | author | Hartsfield JK Jr | Q67570075 |
| P2093 | author name string | Kousseff BG | |
| Hall BD | |||
| Salazar JF | |||
| Grix AW | |||
| Haufe SM | |||
| P2860 | cites work | Cornelia de Lange syndrome. Otolaryngologic manifestations. | Q52055941 |
| A New Dominant Gene Mental Retardation Syndrome | Q56505393 | ||
| P433 | issue | 5 | |
| P921 | main subject | Coffin-Lowry syndrome | Q1106881 |
| pleiotropy | Q1134884 | ||
| P304 | page(s) | 552-557 | |
| P577 | publication date | 1993-03-01 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | Pleiotropy in Coffin-Lowry syndrome: sensorineural hearing deficit and premature tooth loss as early manifestations | |
| P478 | volume | 45 |
| Q51918507 | A case of Coffin-Lowry syndrome with premature exfoliation of primary teeth. |
| Q34811039 | Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes |
| Q34152932 | Coffin-Lowry syndrome: clinical and molecular features |
| Q51907719 | Coffin-Lowry syndrome: findings and dental treatment. |
| Q46614093 | Genes Critical for Developing Periodontitis: Lessons from Mouse Models |
| Q38223091 | Idiopathic gingival fibromatosis associated with progressive hearing loss: A nonfamilial variant of Jones syndrome |
| Q24539742 | Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations |
| Q45961186 | Postmortem findings in the Coffin-Lowry Syndrome. |
| Q41818950 | Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome |
| Q38790109 | Rsk2, the Kinase Mutated in Coffin-Lowry Syndrome, Controls Cementum Formation |
| Q37866350 | Syndromes as they relate to periodontal disease |
| Q33332455 | Systematic analysis of pleiotropy in C. elegans early embryogenesis |
| Q73013123 | X-linked mental retardation |
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