메뉴 건너뛰기




Volumn 64, Issue 1, 1996, Pages 59-62

X-Linked Mental Retardation Syndrome: Three Brothers with the Brooks-Wisniewski-Brown Syndrome

Author keywords

Deeply set eyes; Entropion; New syndrome; Short palpebral fissures; Small mouth; Wide nose tip; X linked mental retardation

Indexed keywords

GENETTA;

EID: 0030011778     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960712)64:1<59::AID-AJMG8>3.0.CO;2-M     Document Type: Article
Times cited : (6)

References (8)
  • 1
    • 0028304863 scopus 로고
    • New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation
    • Brooks SS, Wisniewski K, Brown WB (1994): New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation. Am J Med Genet 51:586-590.
    • (1994) Am J Med Genet , vol.51 , pp. 586-590
    • Brooks, S.S.1    Wisniewski, K.2    Brown, W.B.3
  • 2
    • 0028245481 scopus 로고
    • Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: A new X-linked multiple congenital anomalies/mental retardation syndrome
    • Hamel BCJ, Mariman CM, vanBeersum SEC, Schoonbrood-Lenssen AMJ, Ropers HH (1994): Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: A new X-linked multiple congenital anomalies/mental retardation syndrome. Am J Med Genet 51:591-597.
    • (1994) Am J Med Genet , vol.51 , pp. 591-597
    • Hamel, B.C.J.1    Mariman, C.M.2    VanBeersum, S.E.C.3    Schoonbrood-Lenssen, A.M.J.4    Ropers, H.H.5
  • 3
    • 0026450988 scopus 로고
    • X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family
    • Kang WM, Huang CC, Lin SJ (1992): X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family. Am J Med Genet 44:619-623.
    • (1992) Am J Med Genet , vol.44 , pp. 619-623
    • Kang, W.M.1    Huang, C.C.2    Lin, S.J.3
  • 5
    • 0023625765 scopus 로고
    • X-linked dysmorphic syndrome with mental retardation
    • Prieto F, Badia L, Mulas F, Mora F (1987): X-linked dysmorphic syndrome with mental retardation. Clin Genet 32:326-334.
    • (1987) Clin Genet , vol.32 , pp. 326-334
    • Prieto, F.1    Badia, L.2    Mulas, F.3    Mora, F.4
  • 6
    • 0019219903 scopus 로고
    • Short stature, psychomotor retardation, and unusual facial appearance in two brothers
    • Smith RD, Fineman RM, Myers GG (1980): Short stature, psychomotor retardation, and unusual facial appearance in two brothers. Am J Med Genet 7:5-9.
    • (1980) Am J Med Genet , vol.7 , pp. 5-9
    • Smith, R.D.1    Fineman, R.M.2    Myers, G.G.3
  • 7
    • 0026322752 scopus 로고
    • New X-linked syndrome of mental retardation, short stature and hypertelorism
    • Stoll C, Gerauldel A, Chauvin A (1991): New X-linked syndrome of mental retardation, short stature and hypertelorism. Am J Med Genet 39:474-478.
    • (1991) Am J Med Genet , vol.39 , pp. 474-478
    • Stoll, C.1    Gerauldel, A.2    Chauvin, A.3
  • 8
    • 0026637344 scopus 로고
    • A new XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and dysgenesis of the corpus callosum
    • Zollino M, Mastroiacovo P, Zampino G, Neri G (1992): A new XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and dysgenesis of the corpus callosum. Am J Med Genet 43:452-457.
    • (1992) Am J Med Genet , vol.43 , pp. 452-457
    • Zollino, M.1    Mastroiacovo, P.2    Zampino, G.3    Neri, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.