Sentence examples for linkage in the first from inspiring English sources

Exact(1)

Data linkage in the first instance took place at the GMC, to which was sent by the MRCP UK) and MRCGP office the GMC number, name, date of birth, and place of primary medical qualification of all candidates known to have taken MRCP UK) or MRCGP.

Similar(59)

4 Indicates that number of whole or partial chromosome arms in rainbow trout/Atlantic salmon that are syntenic with the ancestral linkage group designated in the first column.

POMGnT1 is responsible for addition of an N-acetylglucosamine residue in β-1,2 linkage to the first mannose residue.

Although these studies were the best that could be achieved at that stage, these reports should be discounted as there was a substantial bias in the necessity of having a (and more likely several) living affected individual(s) in a family in order to identify linkage to chromosome 17q in the first instance.

Analyses of a cross between two M. graminicola strains that originated from bread wheat fields in The Netherlands resulted in the first genetic linkage map of a Mycosphaerella species [13], [14].

We assume that family trios have been genotyped at a first locus and that the mothers are additionally genotyped at a second locus, both unlinked and in linkage equilibrium with the first locus.

Instead of using rigid multiple degree-of-freedom linkages as fin rays in the first version, six flexible fin rays are adopted to drive two sided fins which generate thrust through flapping motions.

In mammals, the GDP-L-Fuc: N-acetyl-β D-glucosaminide α1,6-fucosyltransferase (α1,6-FucT) is the only enzyme able to catalyze the transfer of a Fuc residue in α1,6-linkage to the first GlcNAc residue of N-glycan chains [ 13].

The six SNPs in linkage disequilibrium at r >0.6 in the first region corresponding to the TERT promoter (that is, rs2736107) were associated with breast cancer risk overall.

In the first linkage study conducted in this area, Smith et al. (1983) focused on a group of nine families in whom dyslexia appeared to be inherited in an autosomal dominant manner.

After the early encouraging findings of the mutations causing the rare Mendelian forms of migraine (familial hemiplegic migraine, FHM) and the loci identified in the first linkage scan for common migraine [ 4], progress has been slow.

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