11 results on '"A Krebsova"'
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2. Embarazo en mujeres portadoras de variantes genéticas de miocardiopatía dilatada
3. Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16
4. Assignment of the Gene for a New Hereditary Nail Disorder, Isolated Congenital Nail Dysplasia, to Chromosome 17p13
5. Distribution of CFTR mutations in the Czech population: Positive impact of integrated clinical and laboratory expertise, detection of novel/de novo alleles and relevance for related/derived populations
6. Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition
7. Identification, by Homozygosity Mapping, of a Novel Locus for Autosomal Recessive Congenital Ichthyosis on Chromosome 17p, and Evidence for Further Genetic Heterogeneity
8. PREGNANCY— ASSOCIATED PLASMA PROTEIN-A AND PROFORM OF EOSINOPHILIC MAJOR BASIC PROTEIN IN THE DETECTION OF ACUTE CORONARY SYNDROME
9. 25. Genotype-phenotype correlations in the CFTRdel21kb mutation in the Czech population
10. 20. A high frequency of the CFTRdel21kb mutation in the Czech population raises the total detection rate to over 95%
11. Genotype/Phenotype Correlation in Autosomal Recessive Lamellar Ichthyosis
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