Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Assman-Hulsmans CF"'
Autor:
Hamel, BC, Smits, AP, de Graaff, E, Smeets, DF, Schoute, F, Eussen, BH, Knight, SJ, Davies, KE, Assman-Hulsmans, CF, Oostra, BA
During an ongoing study on X-linked mental retardation, we ascertained a large family in which mild mental retardation was cosegregating with a fragile site at Xq27-28. Clinical, psychometric, cytogenetic, and molecular studies were performed. Apart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f11f7f9716546f1e11e424a0e0b5efba
https://ora.ox.ac.uk/objects/uuid:b9dd60da-19cf-4d4a-9b9e-af5eaf2bb688
https://ora.ox.ac.uk/objects/uuid:b9dd60da-19cf-4d4a-9b9e-af5eaf2bb688
Autor:
Hamel BC; Department of Human Genetics, University Hospital, Nijmegen, The Netherlands. b.hamel@antrg.azn.nl, Smits AP, van den Helm B, Smeets DF, Knoers NV, van Roosmalen T, Thoonen GH, Assman-Hulsmans CF, Ropers HH, Mariman EC, Kremer H
Publikováno v:
American journal of medical genetics [Am J Med Genet] 1999 Jul 30; Vol. 85 (3), pp. 290-304.
Autor:
Hamel BC; Department of Human Genetics, University Hospital, Nijmegen, The Netherlands., Smits AP, de Graaff E, Smeets DF, Schoute F, Eussen BH, Knight SJ, Davies KE, Assman-Hulsmans CF, Oostra BA
Publikováno v:
American journal of human genetics [Am J Hum Genet] 1994 Nov; Vol. 55 (5), pp. 923-31.