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Volumn 19, Issue 1, 2008, Pages 95-99

Concomitant occurrence of holoprosencephaly and omphalocele

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CHROMOSOME ABERRATION; CLINICAL FEATURE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; GESTATION PERIOD; HOLOPROSENCEPHALY; HUMAN; KARYOTYPING; LETTER; MAJOR CLINICAL STUDY; MALE; OMPHALOCELE; PRENATAL DIAGNOSIS;

EID: 44649158271     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (2)

References (16)
  • 1
    • 0018248640 scopus 로고
    • Sex liability to single structural defects
    • ARENA J.F.P., SMITH D.W.: Sex liability to single structural defects. Am. J. Dis. Child, 1978, 132, 970-972.
    • (1978) Am. J. Dis. Child , vol.132 , pp. 970-972
    • ARENA, J.F.P.1    SMITH, D.W.2
  • 3
    • 0029076262 scopus 로고
    • EUROCAT WORKING GROUP.: Omphalocele and gastroschisis in Europe: a survey of 3 million births 1980-1990
    • CALZOLARI E., BIANCHI F., DOLK H., MILAN M., EUROCAT WORKING GROUP.: Omphalocele and gastroschisis in Europe: a survey of 3 million births 1980-1990. Am. J. Med. Genet., 1995, 58, 187-194.
    • (1995) Am. J. Med. Genet , vol.58 , pp. 187-194
    • CALZOLARI, E.1    BIANCHI, F.2    DOLK, H.3    MILAN, M.4
  • 4
    • 16444376789 scopus 로고    scopus 로고
    • A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly
    • CHEN C.-P., CHERN S.-R., LIN C.-J., LEE C.-C., WANG W., TZEN C.-Y.: A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly. Genet. Counsel., 2005, 16, 49-57.
    • (2005) Genet. Counsel , vol.16 , pp. 49-57
    • CHEN, C.-P.1    CHERN, S.-R.2    LIN, C.-J.3    LEE, C.-C.4    WANG, W.5    TZEN, C.-Y.6
  • 5
    • 34247482797 scopus 로고    scopus 로고
    • Chromosomal abnormalities associated with omphalocele
    • CHEN C.-P.: Chromosomal abnormalities associated with omphalocele. Taiwan. J. Obstet Gynecol., 2007, 46, 1-8.
    • (2007) Taiwan. J. Obstet Gynecol , vol.46 , pp. 1-8
    • CHEN, C.-P.1
  • 6
    • 0029838858 scopus 로고    scopus 로고
    • Holoprosencephaly: Epidemiologic and clinical characteristics of a California population
    • CROEN L.A., SHAW G.M., LAMMER E.J.: Holoprosencephaly: epidemiologic and clinical characteristics of a California population. Am. J. Med. Genet., 1996, 64, 465-472.
    • (1996) Am. J. Med. Genet , vol.64 , pp. 465-472
    • CROEN, L.A.1    SHAW, G.M.2    LAMMER, E.J.3
  • 7
    • 0026604708 scopus 로고
    • Correlation between omphalocele contents and karyotypic abnormalities: Sonographic study in 37 cases
    • GETACHEW M.M., GOLDSTEIN R.B., EDGE V., GOLDBERG J.D., FILLY R.A.: Correlation between omphalocele contents and karyotypic abnormalities: sonographic study in 37 cases. A.J.R., 1992, 158, 133-136.
    • (1992) A.J.R , vol.158 , pp. 133-136
    • GETACHEW, M.M.1    GOLDSTEIN, R.B.2    EDGE, V.3    GOLDBERG, J.D.4    FILLY, R.A.5
  • 8
    • 0023503928 scopus 로고
    • Midline developmental "weakness" as a consequence of determinative field properties
    • LUBINSKY MS.: Midline developmental "weakness" as a consequence of determinative field properties. Am. J. Med. Genet. 1987, 3(suppl.), 23-28.
    • (1987) Am. J. Med. Genet , vol.3 , Issue.SUPPL. , pp. 23-28
    • LUBINSKY, M.S.1
  • 9
    • 0011977665 scopus 로고
    • Holoprosencephaly as a genetic model to study normal craniofacial development
    • MUENKE M.: Holoprosencephaly as a genetic model to study normal craniofacial development. Semin. Dev. Biol., 1994, 5, 293-301.
    • (1994) Semin. Dev. Biol , vol.5 , pp. 293-301
    • MUENKE, M.1
  • 10
    • 0030734649 scopus 로고    scopus 로고
    • Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989
    • OLSEN C.L., HUGHES J.P., YOUNGBLOOD L.G., SHARPE-STIMAC M.: Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989. Am. J. Med. Genet., 1997, 73, 217-226.
    • (1997) Am. J. Med. Genet , vol.73 , pp. 217-226
    • OLSEN, C.L.1    HUGHES, J.P.2    YOUNGBLOOD, L.G.3    SHARPE-STIMAC, M.4
  • 11
    • 0020322650 scopus 로고
    • Editorial comment: CNS anomalies and the midline as a "developmental field
    • OPITZ J.M., GILBERT E.F.: Editorial comment: CNS anomalies and the midline as a "developmental field". Am. J. Med. Genet., 1982, 12, 443-455.
    • (1982) Am. J. Med. Genet , vol.12 , pp. 443-455
    • OPITZ, J.M.1    GILBERT, E.F.2
  • 13
    • 0014329459 scopus 로고
    • Autosomal trisomy syndromes: A detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome
    • TAYLOR A.I.: Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. J. Med. Genet., 1968, 5, 227-252.
    • (1968) J. Med. Genet , vol.5 , pp. 227-252
    • TAYLOR, A.I.1
  • 14
    • 32244442921 scopus 로고    scopus 로고
    • Three-dimensional first-trimester transvaginal diagnosis of alobar holoprosencephaly associated with omphalocele in a 46,XX fetus
    • TONNI G., CENTINI G.: Three-dimensional first-trimester transvaginal diagnosis of alobar holoprosencephaly associated with omphalocele in a 46,XX fetus. Am. J. Perinatol., 2006, 23, 67-69.
    • (2006) Am. J. Perinatol , vol.23 , pp. 67-69
    • TONNI, G.1    CENTINI, G.2
  • 15
    • 0013978242 scopus 로고
    • Congenital malformations in autosomal trisomy syndromes
    • WARKANY J., PASSARGE E., SMITH L.B.: Congenital malformations in autosomal trisomy syndromes. Am. J. Dis. Child., 1966, 112, 502-517.
    • (1966) Am. J. Dis. Child , vol.112 , pp. 502-517
    • WARKANY, J.1    PASSARGE, E.2    SMITH, L.B.3
  • 16
    • 0030035711 scopus 로고    scopus 로고
    • Holoprosencephaly in the west of Scotland. 1975-1994
    • WHITEFORD M.L., TOLMIE J.L.: Holoprosencephaly in the west of Scotland. 1975-1994. J. Med. Genet., 1996, 33, 578-584.
    • (1996) J. Med. Genet , vol.33 , pp. 578-584
    • WHITEFORD, M.L.1    TOLMIE, J.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.