27 results on '"Grisart, Bernard"'
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2. Genetic and Functional Confirmation of the Causality of the DGAT1 K232A Quantitative Trait Nucleotide in Affecting Milk Yield and Composition
3. Fine-Mapping of Quantitative Trait Loci by Identity by Descent in Outbred Populations: Application to Milk Production in Dairy Cattle
4. Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges
5. Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations.
6. Outcome of publicly funded nationwide first-tier noninvasive prenatal screening.
7. Le Diagnostic Prénatal Non Invasif sur cellules fœtales :Mythe ou réalité ?
8. Molecular dissection of a quantitative trait locus: a phenylalanine-to-tyrosine substitution in the transmembrane domain of the bovine growth hormone receptor is associated with a major effect on milk yield and composition
9. Simultaneous mining of linkage and linkage disequilibrium to fine map quantitative trait loci in outbred half-sib pedigrees: revisiting the location of a quantitative trait locus with major effect on milk production on bovine chromosome 14
10. Spectrum of Mutations in Gitelman Syndrome
11. A rank-based nonparametric method for mapping quantitative trait loci in outbred half-sib pedigrees: application to milk production in a granddaughter design
12. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.
13. Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15-year-old girl.
14. Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.
15. Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15‐year‐old girl
16. Positional candidate cloning of a QTL in dairy cattle: identification of a missense mutation in the bovine DGATI gene with major effect on milk yield and composition
17. Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges
18. five Int22h Homologous Copies in Association with Intron22 Inversion Type 3
19. Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1–q25.32: Genotype–phenotype correlations of chromosome 3q25 deletion syndrome
20. Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.
21. Deletion of KDM6A, a histone demethylase interacting with MLL2, in three patients with kabuki syndrome
22. Intron 22 homologous regions are implicated in exons 1–22 duplications of the F8 gene
23. Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome
24. NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?
25. Cinétique de développement et activité transcriptionnelle de l'embryon bovin produit in vitro
26. Extensive Genome-wide Linkage Disequilibrium in Cattle
27. Molecular Dissection of a Quantitative Trait Locus: A Phenylalanine-Tyrosine Substitution in the Transmembrane Domain of the Bovine Growth Hormone Receptor Is Associated With a Major Effect on Milk Yield and Composition.
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