Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Efraim, Gazit"'
Publikováno v:
Anthropologischer Anzeiger. 62:147-155
The 844ins68 allele in the cystathionine beta-synthase gene is always found in cis with the T833C mutation further indicating that its origin is monophyletic and that it might be a useful anthropogenetic marker. Its frequency was examined in 1087 ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8927d8f8f23105aeb475fb5e2b0dfa9
https://doi.org/10.1127/anthranz/62/2004/147
https://doi.org/10.1127/anthranz/62/2004/147
Publikováno v:
Anthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur. 62(2)
The 844ins68 allele in the cystathionine beta-synthase gene is always found in cis with the T833C mutation further indicating that its origin is monophyletic and that it might be a useful anthropogenetic marker. Its frequency was examined in 1087 ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f9ca5bf96162388c389b1da283aff07
https://pubmed.ncbi.nlm.nih.gov/15228193
https://pubmed.ncbi.nlm.nih.gov/15228193
Publikováno v:
Pediatric Research. 11:1129-1132
Summary: This study reports a serologic method for the measurement of kidney-derived antigens in the urine of healthy children and of children with renal diseases. Two hundred twenty patients were studied. Four groups were recognized: group A, patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed91ffae0243825896df4f353f20f01
https://doi.org/10.1203/00006450-197711000-00002
https://doi.org/10.1203/00006450-197711000-00002
Publikováno v:
Pediatric Research. 19:253A-253A
Cohen syndrome, a congenital disorder first described in 1973, is characterized by universal occurrence of mental retardation of variable degree and facial anomalies (short filtrum, high nasal bridge, high arched palate, prominent central incisors, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9c3df0410d55a2e324d4349df757b4c
https://doi.org/10.1203/00006450-198504000-00885
https://doi.org/10.1203/00006450-198504000-00885