Pages that link to "Q35200364"
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The following pages link to Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information (Q35200364):
Displaying 35 items.
- Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium (Q24670212) (← links)
- The use of neurophysiological endophenotypes to understand the genetic basis of schizophrenia. (Q30473421) (← links)
- Familial screening for genetic haemochromatosis by means of DNA markers (Q33863012) (← links)
- Neurofibromatosis type 1 (NF1): knowledge, experience, and reproductive decisions of affected patients and families (Q33595557) (← links)
- Genetic linkage analysis of a dichotomous trait incorporating a tightly linked quantitative trait in affected sib pairs (Q33905107) (← links)
- The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness (Q33994157) (← links)
- Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivity. (Q34122468) (← links)
- Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. I. Likelihood formulation and simulation results (Q34145764) (← links)
- HLA determinants in an Australian population of hemochromatosis patients and their families (Q35197328) (← links)
- Segregation of genetic hemochromatosis indexed by latent capacity of transferrin (Q35197396) (← links)
- Sample-size guidelines for linkage analysis of a dominant locus for a quantitative trait by the method of lod scores (Q35198098) (← links)
- Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLA. (Q35198463) (← links)
- Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies. (Q35246930) (← links)
- Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE) (Q35889091) (← links)
- Combined segregation and linkage analysis of Graves disease with a thyroid autoantibody diathesis. (Q35889681) (← links)
- Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus (Q35956504) (← links)
- Allelic association under map error and recombinational heterogeneity: a tale of two sites (Q36310508) (← links)
- Deconstructing schizophrenia: an overview of the use of endophenotypes in order to understand a complex disorder (Q36646593) (← links)
- Current perspectives on the genetics of unipolar depression (Q37218496) (← links)
- Missing heritability of complex diseases: Enlightenment by genetic variants from intermediate phenotypes (Q37340699) (← links)
- Toward a modern search for schizophrenia genes (Q38578844) (← links)
- Assessing the role of HLA-linked and unlinked determinants of disease (Q40593830) (← links)
- A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA as (Q40600636) (← links)
- Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE). (Q48068018) (← links)
- Eye movement abnormality suggestive of a spatial working memory deficit is present in parents of autistic probands (Q50345904) (← links)
- [Endophenotype--a new concept for biological characterization of psychiatric disorders]. (Q53260719) (← links)
- Ferritin H gene polymorphism in idiopathic hemochromatosis (Q57203408) (← links)
- Reproduction démographique et transmission génétique dans le nord-est de la province de Québec (XVIIIe-XXe siècles) (Q57305467) (← links)
- Segregation analysis of NIDDM in Caucasian families (Q57919797) (← links)
- Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia (Q63386330) (← links)
- Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis (Q67516177) (← links)
- Detection of hereditary haemochromatosis in an HLA-identical pedigree showing discordance between HLA class I genes and the disease locus (Q67792089) (← links)
- HLA class I gene polymorphism in genetic hemochromatosis (Q68094833) (← links)
- Genetic hemochromatosis and HLA linkage (Q68770479) (← links)
- DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family (Q69888665) (← links)