| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1399-0004.1995.TB04307.X |
| P698 | PubMed publication ID | 7554352 |
| P50 | author | Alain Verloes | Q64955175 |
| P2093 | author name string | L Koulischer | |
| J P Langhendries | |||
| B Massart | |||
| I Dehalleux | |||
| P433 | issue | 5 | |
| P304 | page(s) | 257-262 | |
| P577 | publication date | 1995-05-01 | |
| P1433 | published in | Clinical Genetics | Q5133760 |
| P1476 | title | Clinical overlap of Beckwith-Wiedemann, Perlman and Simpson-Golabi-Behmel syndromes: a diagnostic pitfall | |
| P478 | volume | 47 |
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| Q41825402 | Differential effects of Th1, monocyte/macrophage and Th2 cytokine mixtures on early gene expression for glial and neural-related molecules in central nervous system mixed glial cell cultures: neurotrophins, growth factors and structural proteins |
| Q37517229 | Hypothesis: a new role for the Renin-Angiotensin system in ureteric bud branching |
| Q35197831 | Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes |
| Q24320198 | Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome |
| Q36255453 | OCI-5/GPC3, a glypican encoded by a gene that is mutated in the Simpson-Golabi-Behmel overgrowth syndrome, induces apoptosis in a cell line-specific manner. |
| Q33997957 | Perilobar nephroblastomatosis: natural history and management |
| Q57839628 | Perlman syndrome—a cause of enlarged, hyperechogenic kidneys |
| Q73013123 | X-linked mental retardation |
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