28 results on '"Eiberg H"'
Search Results
2. Identification of novel locus at chromosome 3p12.3-q13.31 for autosomal recessive intellectual disability in a consanguineous family
3. Genetic heterogeneity in Pakistani microcephaly families
4. Genetic studies in congenital anterior midline cervical cleft
5. Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)
6. RUNX2 analysis of Danish cleidocranial dysplasia families
7. Autosomal dominant congenital cataract Morphology and genetic mapping
8. Polymorphic drug metabolizing CYP-enzymes - a pathogenic factor in oral lichen planus?
9. Batten disease (Spielmeyer-Sjogren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16
10. Linkage between serum cholinesterase 2 (CHE2) and γ-crystallin gene cluster (CRYG): assignment to chromosome 2
11. Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
12. Confirmation of F13A assignment and sequence information concerning F13A-HLA-GLO
13. Δ-Aminolevulinatedehydrase: synteny with ABO-AK1-ORM (and assignment to chromosome 9)
14. Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22
15. Linkage between the loci for cystic fibrosis and paraoxonase
16. Molecular genetics of nocturnal enuresis: clinical and genetic heterogeneity
17. Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation
18. Heterogeneity of FeNO response to inhaled steroid in asthmatic children
19. Molecular genetic, clinical and psychiatric associations in nocturnal enuresis
20. Suggestion of linkage between manic‐depressive illness and the enzyme phosphoglycolate phosphatase (PGP) on chromosome 16p
21. Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material
22. Proposal for the Nomenclature of Human Plasminogen (PLG) Polymorphism
23. Genetics of paraoxonase
24. Linkage relationships of paraoxonase (PON) with other markers: indication of PON‐cystic fibrosis synteny
25. Linkage of plasma α‐L‐fucosidase (FUCA2) and the plasminogen (PLG) system
26. Cystic fibrosis; hint of linkage with F13B
27. Gentics and linkage relationships of the C3 polymorphism: discovery of C3‐Se linkage and assignment of LES‐C3‐DM‐Se‐PEPD‐Lu synteny to chromosome 19
28. The influence of parental history of diabetes and offspring birthweight on offspring glucose metabolism in adulthood.
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