11 results on '"Wilson, Louise C."'
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2. Cover Image, Volume 176A, Number 4, April 2018
3. Natural history and genotype‐phenotype correlations in 72 individuals with SATB2 ‐associated syndrome
4. Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype
5. Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199-214 cluster in the skeletal features of the condition
6. Frontometaphyseal dysplasia and keloid formation withoutFLNAmutations
7. A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype
8. Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
9. Type 1 collagenopathy presenting with a Russell-Silver phenotype
10. Molecular and clinical characterization of cardio-facio-cutaneous (CFC) syndrome: Overlapping clinical manifestations with Costello syndrome
11. Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization of 11 cases
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