19 results on '"Murray, J.C."'
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2. Mutation and deletion analysis of the Van der Woude syndrome locus at chromosome 1q32-q41
3. Heterozygous PITX2/RIEG1 gene deletion associated with GH deficiency in Rieger syndrome
4. A new phenotype of familial visceral inversus/atrial fibrillation/ASD caused by a novel 7bp deletion in the CSX/NKX2.5 gene
5. TGFA is a genetic modifier of Van der Woude Syndrome
6. A Low Density Lipoprotein Receptor Related Protein-Associated Protein 1 Del/ Ins Polymorphism and Phenotypic Variability in Alzheimer Disease
7. Candidate gene analysis of cleft lip/palate with hypodontia outside the cleft
8. A TDT and candidate analysis shows TGFB3 involved in non-syndromic clefting in an Asian population
9. Mutations in MSX1 are associated with Non-Syndromic Orofacial Clefting
10. MSX1 Variant is Associated with Cleft Lip/Palate in a South American Population
11. Genetic susceptibility to preeclampsia: evaluation of eNos, TGFB3, and AGT mutations
12. Domain-Specific Mutations in the Human Transforming Growth Factor Beta 1 Gene (TGFB1) Result in Camurati-Engelmann Disease
13. Characterization of two unusual polymorphisms identified by sequence comparison
14. Identity by descent and candidate gene mapping of Richieri-Costa- Pereira syndrome
15. Characterization of 41 genes identified through the analysis of 1 Mb of sequence surrounding the Van der Woude sydrome (VWS) critical region at 1q32
16. A 700 kb contig of sequence-ready bacterial clones from mouse chromosome 1H spanning the syntenic region for the Van der Woude syndrome locus at human chromosome 1q32-q41
17. Association of MSX1 with Nonsyndromic Orofacial Clefting in ECLAMC
18. Identification of a dominant negative Rieger syndrome mutation in PITX2
19. Analysis of the p63 Gene in Classic EEC Syndrome, Related Syndromes, and Nonsyndromic Orofacial Clefts
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