Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 4 de 4
Filtrer
Plus de filtres









Sujet principal
Gamme d'année
1.
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
Hagens O; Dubos A; Abidi F; Barbi G; Van Zutven L; Hoeltzenbein M; Tommerup N; Moraine C; Fryns JP; Chelly J; Van Bokhoven H; Gécz J; Dollfus H; Ropers HH; Schwartz CE; Stocco RC; Hanauer A.
Hum Gene ; 118(5): p.578-90, 2006.
Article de Anglais | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib10503

Sujet(s)
Génétique
2.
Stocco dos Santos X-linked mental retardation syndrome: Clinical elucidation and localization to Xp11.3-Xq21.3.
dos Santos RCS; Castro NHC; Holmes AL; Beçak, Willy; Tackels-Horne D; Lindsey CJ; Lubs HÁ; Stevenson RE; Schwartz CE.
Am J Med Genet A ; 118A(3): p.255-9, 2003.
Article de Anglais | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib12955

Sujet(s)
Génétique
3.
Shashi XLMR syndrome: Report of a second family
Castro NHC; dos Santos RCS; Nelson R; Beçak, Willy; Hane B; Lindsey CJ; Lubs HÁ; Stevenson RE; Schwartz CE.
Am J Med Genet A ; 118A(1): p.49-51, 2003.
Article de Anglais | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib12835

Sujet(s)
Génétique
4.
Parting Company: Understanding the Loss of a Loved One. The Caregiver's Journey.
Schwartz CE.
Ann Intern Med ; 133(7): 572, 2000 Oct 03.
Article de Anglais | MEDLINE | ID: mdl-11015185
ENVOYER À:
Email
Exporter
Imprimer
RSS
XML
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE