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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 in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib10503

Subject(s)
Genetics
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 in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib12955

Subject(s)
Genetics
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 in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib12835

Subject(s)
Genetics
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 in English | MEDLINE | ID: mdl-11015185
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