CASPubMedGoogle Scholar Kleczkowska, A., Dmoch, E., Kubein, E., Fryns, J.P., and Van den Berghe, H. (1990) Cytogenetic findings in a consecutive series of 478 patients with Turner’s syndrome. The Lueven experience.Genet. Couns.1, 227–233. CASPubMedGoogle Scholar Nielsen J. and...
Conclusion: This is the largest available series of human oocytes tested for live chromosomes most commonly involved in age-related aneuphlidies, demonstrating 52.1% rate of chromosomal abnormalities originating equally from errors in meiosis I and II. The data suggest that avoiding the transfer of ...
chromosomal aberration (redirected fromChromosome abnormalities) Thesaurus Medical Encyclopedia Wikipedia ThesaurusAntonymsRelated WordsSynonymsLegend: Switch tonew thesaurus Noun1.chromosomal aberration- any change in the normal structure or number of chromosomes; often results in physical or mental abnormalities...
To the best of our knowledge, there were no large series of 45,X cases has been reported from Indonesia. Ninety five cases with 45,X cell line found, of which 60 were detected by karyotyping, 4 by FISH for sex chromosomes, and 31 by both karyotyping and FISH. Using karyotyping 37 out...
The effectiveness of a psychological treatment tends to corroborate the finding, drawn from descriptive series, that abnormal sex chromosomes are relatively unimportant as determinants of psychosexual disorders. Moreover, the presence of sex chromosome abnormalities in psychosexual disorders would appear to ...
Ethylhydrocupreine is the most recent of a series of quinine derivatives to be cited for its value in the treatment for pneumonia. That the drug is used quite extensively is shown by Crosswho reported observations made in 126 cases of pn... CM Swab - 《Archives of Ophthalmology》 被引量...
Kokosi MA, Margaritopoulos GA, Wells AU (2018) Personalised medicine in interstitial lung diseases: Number 6 in the Series “Personalised medicine in respiratory diseases” Edited by Renaud Louis and Nicolas Roche. Eur Respir Rev 27(148):170117 Article PubMed Google Scholar Gruden JF, Naidich...
No mutations in γ-catenin, AXIN1 and 2 genes were detected in this series. Neither RAS mutations nor phospho-Akt expression, which were found in 16 and 27.6% of the cases, respectively, were associated with β-catenin nuclear expression. Our results demonstrated a high prevalence of ...
Bertrand Y, Muller SM, Casanova JL et al (2002) Reticular dysgenesis: Hla non-identical bone marrow transplants in a series of 10 patients. Bone Marrow Transplant 29: 759–762 ArticlePubMedGoogle Scholar Roper M, Parmley RT, Crist WM et al (1985) Severe congenital leukopenia (reticular dysg...
A series of 100 modified Kremer tests of sperm penetration into cervical was carried out as part of the routine investigation of couples presenting with . ... D Mortimer,Pandya, I. J,Sawers, R. S - 《Journal of Reproduction & Fertility》 被引量: 245发表: 1986年 加载更多来源...