Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Kefalas, K."'
Publikováno v:
Flora Mediterranea; 2022, Vol. 32, p35-45, 11p
Autor:
Stamatiou, K., Bleibel, A., Valasis, G., Simatos, G., Tsavari, E., Koulia, K., Mourmouras, N., Kefalas, K.
Publikováno v:
Scientific Chronicles / Epistimonika Chronika; 2021, Vol. 26 Issue 4, p599-605, 7p
New information has extended the known range of Callitriche pulchra Schotsm. (Plantaginaceae) to Cyprus. This, combined with a survey of populations on the island of Gavdos off the S coast of Crete, shows that it is less threatened than previously th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::bc76d135c8af533c40e7bd5ccedb2a7d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3058618
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3058618
We report on a 27 month old boy presenting with psychomotor delay and dysmorphic features, mainly mild facial asymmetry, prominent cup-shaped ears, long eyelashes, open mouth appearance and slight abnormalities of the hands and feet. Array comparativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::742b0cff631cfa53ad47f1e3c26f1c24
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088761
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088761
Proximal 10q duplication is a well- defined but rare genetic syndrome. Duplication of proximal segments of the long arm of chromosome 10 results in a pattern of malformations, which are distinct from those of the more common distal 10q trisomy syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::670843f683fbe0793038de8b2e364ae3
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3001698
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3001698
We report on a 26-month-old boy with an interstitial duplication of 2p22.3p22.2 and an interstitial deletion of 2q14.1q21.2. The abnormality was derived from his father having a balanced paracentric inversion and pericentric insertion. The deletion i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::b478d97af4dcb3e7d5e4b83eb3e82f40
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088933
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088933
Background: The 4q- syndrome is a well known genetic condition caused by a partial terminal or interstitial deletion in the long arm of chromosome 4. The great variability in the extent of these deletions and the possible contribution of additional g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::01f434d29df0f1add1561c869b637517
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088612
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3088612
Small supernumerary marker chromosomes (sSMCs) cannot be identified or characterized unambiguously by conventional cytogenetic banding techniques. Until recently, the large variety of marker chromosomes, as well as the limitations in their identifica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::68c9651394b1f721b4fbe88815ae8c20
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3090589
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3090589
Background. The genetic diagnosis of mental retardation (MR) is difficult to establish and at present many cases remain undiagnosed and unexplained. Standard karyotyping has been used as one of the routine techniques for the last decades. The impleme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e0cdf56adbcff8f9267e67dba67f0b33
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3090015
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3090015