16 results on '"Grimm T"'
Search Results
2. Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD)
3. Fabry's disease: Heterozygote detection by hair root analysis
4. Reciprocal or nonreciprocal human chromosome translocations?: The identification of reciprocal translocations by silver staining
5. Chromosome 7 short arm deletion, 7p21→pter
6. Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families
7. Crossing-over during human spermatogenesis visualized cytologically
8. Genetic counseling in families with spinal muscular atrophy type Kugelberg-Welander
9. Familial Robertsonian translocation t13q/15q
10. Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families
11. Heterozygote tests and genetic counseling in Maple Syrup Urine Disease
12. Patterns of deletions of the dystrophin gene in different European populations.
13. Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.
14. No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.
15. The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II.
16. Variable composition of X chromosomal mosaics: due to asynchronous cell division during early embryogenesis?
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