Zobrazeno 1 - 10
of 13
pro vyhledávání: '"K.R. Manjunatha"'
Publikováno v:
International Journal of Human Genetics. 10:33-39
A majority of subjects with mental retardation and congenital anomalies cannot be classified under anyknown malformation syndromes. Major problems in understanding the mechanisms involved in the pr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a372498be42da090e52edc357a5f06f
https://doi.org/10.1080/09723757.2010.11886082
https://doi.org/10.1080/09723757.2010.11886082
Publikováno v:
International Journal of Human Genetics. 2:61-64
KEY WORDSCytogenetics; association; absolutes. ABSTRACT The frequency and pattern of satellite association was studied in lymphocyte culture of couples with recurrent spontaneous abortions and control popu- lation. A statistically highly significant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a048feb06851e1635b730065a8d76ef7
https://doi.org/10.1080/09723757.2002.11885786
https://doi.org/10.1080/09723757.2002.11885786
Autor:
G.V. Bhaskara Rao, G.K. Chetan, Shoba Srinath, S. Padma, S.R. Girimaji, K.R. Manjunatha, Sheshadri Sp, R. Arathi, H.N. Venkatesh, P. Latha
Publikováno v:
International Journal of Human Genetics. 2:33-39
Population studies have shown that over- all prevalence of mild to severe mental retardation ranges from 2.5 to 5 per thousand. Genetic contribution to this group accounts for 15-30%. The role of chromosomal fragile sites in cancer, recurrent abortio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9167dfe949450a966cf89072b5952dec
https://doi.org/10.1080/09723757.2002.11885781
https://doi.org/10.1080/09723757.2002.11885781
Autor:
R. Arathi, H.N. Venkatesh, S.R. Girimaji, Shoba Srinath, Sheshadri Sp, K.R. Manjunatha, S. Padma, G.K. Chetan
Publikováno v:
International Journal of Human Genetics. 1:293-299
Autism is a behavioural disorder in chil- dren with male predominance. The genetic basis of autism is now well established with twin and family studies. Association of autosomal fragile sites play an important role in the absence of any other genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6df7dc5c32da398205edeca6e4ed2cea
https://doi.org/10.1080/09723757.2001.11885773
https://doi.org/10.1080/09723757.2001.11885773
Autor:
G.V. Bhaskar Rao, S. Padma, R. Arathi, H.N. Venkatesh, G.K. Chetan, S.R. Girimaji, P. Latha, K.R. Manjunatha
Publikováno v:
International Journal of Human Genetics. 1:91-95
Fragile X chromosome screening was un- dertaken among 100 non-specific mentally retarded group from the Indian population. 14 subjects from 10 families showed the presence of fragile X chromosomes in 4 to 40% of cells. Various 'C' group autosomes sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1451921fca470f14ca4d609954af774
https://doi.org/10.1080/09723757.2001.11885740
https://doi.org/10.1080/09723757.2001.11885740
Publikováno v:
Genomics and Health in the Developing World
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39a3d535aba19de15d77ae579e7e6a9c
https://doi.org/10.1093/med/9780195374759.003.0095
https://doi.org/10.1093/med/9780195374759.003.0095
Publikováno v:
International Journal of Human Genetics. 1:191-193
An increased frequency of mitoses with centromere separation affecting all chromosomes was found in lymphocyte cultures of couples with recurrent spontaneous abortions. This anomaly was recorded in six individuals out of seventy couples (one hundred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b6c85fb7ca0b690c7433324c48766f1
https://doi.org/10.1080/09723757.2001.11885758
https://doi.org/10.1080/09723757.2001.11885758
Autor:
S. Padma, H.N. Venkatesh, G.K. Chetan, R. Arathi, S. Shobha, V. Shobha, P. Latha, G.V. Bhakar Rao, Sheshadri Sp, S.R. Girimaji, K.R. Manjunatha
Publikováno v:
INTERNATIONAL JOURNAL OF HUMAN GENETICS.
Fragile X syndrome is the commonest form of X-linked disorder. Its frequency among MR ranges from 6-9%. There are a few reports available on Fragile X syndrome from Indian population and we have screened for 300 MR subjects with 26 subjects (8.6%) sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f301df55a553c3f203f71a7fcba1ce82
https://doi.org/10.31901/24566330.2002/02.02.01
https://doi.org/10.31901/24566330.2002/02.02.01
Autor:
K.R. Manjunatha
Publikováno v:
INTERNATIONAL JOURNAL OF HUMAN GENETICS.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de39565c0cd465cee5ee600030c0196b
https://doi.org/10.31901/24566330.2002/02.01.07
https://doi.org/10.31901/24566330.2002/02.01.07
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