Pages that link to "Q30513809"
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The following pages link to John W. Belmont (Q30513809):
Displaying 50 items.
- European population substructure: clustering of northern and southern populations (Q21092502) (← links)
- Low levels of genetic divergence across geographically and linguistically diverse populations from India (Q21145243) (← links)
- SNP genotyping to screen for a common deletion in CHARGE syndrome (Q21261454) (← links)
- Analysis of East Asia genetic substructure using genome-wide SNP arrays (Q21562489) (← links)
- Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development. (Q22008848) (← links)
- Genome-wide detection and characterization of positive selection in human populations (Q23000444) (← links)
- CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs (Q24312161) (← links)
- Characterization of the interactions of human ZIC3 mutants with GLI3 (Q24338829) (← links)
- Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects (Q24533160) (← links)
- Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation (Q24540535) (← links)
- Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay (Q24557419) (← links)
- SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing (Q24614096) (← links)
- Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly (Q24642861) (← links)
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities (Q24647145) (← links)
- A second generation human haplotype map of over 3.1 million SNPs (Q24651939) (← links)
- Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis (Q24791336) (← links)
- Positive selection of a pre-expansion CAG repeat of the human SCA2 gene (Q24810496) (← links)
- Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy (Q28185174) (← links)
- Localization of BRRN1, the Human Homologue ofDrosophila barr,to 2q11.2 (Q28258101) (← links)
- Prenatal diagnosis and treatment of holocarboxylase synthetase deficiency (Q28373907) (← links)
- Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway (Q28594057) (← links)
- The futility of genomic counseling: essential role of electronic health records (Q28752658) (← links)
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size (Q29544005) (← links)
- Prior infections with seasonal influenza A/H1N1 virus reduced the illness severity and epidemic intensity of pandemic H1N1 influenza in healthy adults (Q30409342) (← links)
- Antibody correlates and predictors of immunity to naturally occurring influenza in humans and the importance of antibody to the neuraminidase (Q30425783) (← links)
- Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions (Q30502924) (← links)
- NPHP4 variants are associated with pleiotropic heart malformations (Q30571081) (← links)
- Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort (Q31149204) (← links)
- Identification and cloning of differentially expressed genes by long-distance differential display (Q32061691) (← links)
- The Twiddling Andersen (Q33157711) (← links)
- An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels (Q33486736) (← links)
- Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping (Q33519737) (← links)
- The molecular basis of vascular disorders (Q33537697) (← links)
- BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects (Q33677028) (← links)
- "Personalizing" academic medicine: opportunities and challenges in implementing genomic profiling (Q33698028) (← links)
- Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections (Q33940731) (← links)
- Long-distance DD-PCR and cDNA microarrays (Q33941550) (← links)
- Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome). (Q34047018) (← links)
- Genetic basis of congenital cardiovascular malformations (Q34125381) (← links)
- Molecular determinants of left and right outflow tract obstruction (Q34263600) (← links)
- Omphalocele in trisomy 3q: further delineation of phenotype (Q34276738) (← links)
- Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci. (Q34301488) (← links)
- Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001 (Q34338168) (← links)
- Rare copy number variants disrupt genes regulating vascular smooth muscle cell adhesion and contractility in sporadic thoracic aortic aneurysms and dissections (Q34381768) (← links)
- Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy (Q34516932) (← links)
- Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning (Q34582831) (← links)
- Identification of a novel role of ZIC3 in regulating cardiac development (Q34623946) (← links)
- Array-based DNA diagnostics: let the revolution begin (Q34706763) (← links)
- 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome (Q34733853) (← links)
- Early patterns of gene expression correlate with the humoral immune response to influenza vaccination in humans (Q34743359) (← links)