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Volumn 7, Issue 3, 1998, Pages 213-216

Association of holoprosencephaly, ectrodactyly, cleft lip/cleft palate and hypertelorism: A possible third case

Author keywords

Cleft lip cleft palate; Ectrodactyly; Holoprosencephaly; Hypertelorism; New association

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLEFT LIP PALATE; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; ECTRODACTYLY; FAMILY HISTORY; HOLOPROSENCEPHALY; HUMAN; HYPERTELORISM; MALE; PRIORITY JOURNAL;

EID: 0031847202     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199807000-00011     Document Type: Article
Times cited : (11)

References (10)
  • 1
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    • Apparently new oculo-crebro-acral syndrome
    • Atkin JF, Patil S (1984). Apparently new oculo-crebro-acral syndrome. Am J Med Genet 19:585-587.
    • (1984) Am J Med Genet , vol.19 , pp. 585-587
    • Atkin, J.F.1    Patil, S.2
  • 2
    • 4244216018 scopus 로고
    • Interstitial deletion of 2q24.3-q31.1 causes characteristic distal limb malformations
    • Boles RG, Prober BR, McGrath J, Yang-Feng TL (1993). Interstitial deletion of 2q24.3-q31.1 causes characteristic distal limb malformations. Am J Hum Genet 53 (Suppl.):A406.
    • (1993) Am J Hum Genet , vol.53 , Issue.SUPPL.
    • Boles, R.G.1    Prober, B.R.2    McGrath, J.3    Yang-Feng, T.L.4
  • 4
    • 0021710202 scopus 로고
    • Syndrome identification case report 119. Hypertelorism associated with holoprosencephaly and ectrodactyly
    • Hartsfield JK, Bixler D, DeMyer WE (1984). Syndrome identification case report 119. Hypertelorism associated with holoprosencephaly and ectrodactyly. J Clin Dysmorphol 2:27-31.
    • (1984) J Clin Dysmorphol , vol.2 , pp. 27-31
    • Hartsfield, J.K.1    Bixler, D.2    DeMyer, W.E.3
  • 5
    • 15444354176 scopus 로고
    • Further evidence for the presence of a split hand/foot deformity gene on chromosome 7q21 from a segregation a 2;7 translocation
    • Neri G, Genuardi M, Pomponi MG, Sammito V, Zollino M (1992). Further evidence for the presence of a split hand/foot deformity gene on chromosome 7q21 from a segregation a 2;7 translocation. Am J Hum Genet 51 (Suppl.):A327.
    • (1992) Am J Hum Genet , vol.51 , Issue.SUPPL.
    • Neri, G.1    Genuardi, M.2    Pomponi, M.G.3    Sammito, V.4    Zollino, M.5
  • 7
    • 0029040985 scopus 로고
    • Ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosum
    • Saal HM, Bulas DI (1995). Ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosum. Clin Dysmorphol 4:246-250.
    • (1995) Clin Dysmorphol , vol.4 , pp. 246-250
    • Saal, H.M.1    Bulas, D.I.2
  • 8
    • 84876816454 scopus 로고
    • Fine mapping of the autosomal dominant split hand/foot locus on chromosome 7, band q21.3-q22.1
    • Scherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M et al. (1994). Fine mapping of the autosomal dominant split hand/foot locus on chromosome 7, band q21.3-q22.1. Am J Hum Genet 55:12-20.
    • (1994) Am J Hum Genet , vol.55 , pp. 12-20
    • Scherer, S.W.1    Poorkaj, P.2    Allen, T.3    Kim, J.4    Geshuri, D.5    Nunes, M.6
  • 9
    • 0026435070 scopus 로고
    • Holoprosencephaly, telecanthus and ectrodactyly: A second case
    • Young ID, Zuccollo JM, Barrow M, Fowlie A (1992). Holoprosencephaly, telecanthus and ectrodactyly: a second case. Clin Dysmorphol 1:47-51.
    • (1992) Clin Dysmorphol , vol.1 , pp. 47-51
    • Young, I.D.1    Zuccollo, J.M.2    Barrow, M.3    Fowlie, A.4
  • 10
    • 0027182938 scopus 로고
    • Split foot anomaly, microphthalmia, cleft lip and cleft palate and mental retardation associated with a chromosome 6:13 translocation
    • Viljoen DL, Smart R (1993). Split foot anomaly, microphthalmia, cleft lip and cleft palate and mental retardation associated with a chromosome 6:13 translocation. Clin Dysmorphol 2:274-277.
    • (1993) Clin Dysmorphol , vol.2 , pp. 274-277
    • Viljoen, D.L.1    Smart, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.