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Volumn 11, Issue 1, 2000, Pages 61-62

Cystic hygroma colli in triplo-X syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CYSTIC LYMPHANGIOMA; FEMALE; FETUS; FETUS MALFORMATION; HUMAN; HUMAN CELL; KARYOTYPE 47,XXX; TRIPLO X SYNDROME;

EID: 0034050912     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (14)
  • 1
    • 0014665910 scopus 로고
    • The triplo-X female: An appraisal based on a study of 12 cases and a review of the literature
    • BARR M.L., SERGOVICH F.R., CARR D.H., SAVER E.L. : The triplo-X female: an appraisal based on a study of 12 cases and a review of the literature. Can. Med. Assoc. J., 1969, 101, 247-258.
    • (1969) Can. Med. Assoc. J. , vol.101 , pp. 247-258
    • Barr, M.L.1    Sergovich, F.R.2    Carr, D.H.3    Saver, E.L.4
  • 2
    • 0343925753 scopus 로고
    • Clinical and cytogenetic studies on a group of females with XXX sex chromosome complements
    • DAY R.W., LARSON W., WRIGHT S.W.: Clinical and cytogenetic studies on a group of females with XXX sex chromosome complements. J. Pediatr., 1964, 64, 24-33.
    • (1964) J. Pediatr. , vol.64 , pp. 24-33
    • Day, R.W.1    Larson, W.2    Wright, S.W.3
  • 3
    • 0020596511 scopus 로고
    • X-chromosome polysomy in the female: Personal experience and review of the literature
    • FRYNS J.P., KLECZKOWSKA A., PETIT P., VAN DEN BERGHE H.: X-chromosome polysomy in the female: personal experience and review of the literature. Clin. Genet., 1983, 23, 341-349.
    • (1983) Clin. Genet. , vol.23 , pp. 341-349
    • Fryns, J.P.1    Kleczkowska, A.2    Petit, P.3    Van Den Berghe, H.4
  • 4
    • 0028935164 scopus 로고
    • The karyotype of fetuses with anomalies detected by second trimester ultrasonography
    • GONEN R., DAR H., DEGANI S.: The karyotype of fetuses with anomalies detected by second trimester ultrasonography. Eur. J. Obstet. Gynecol. Reprod. Biol., 1995, 58, 153-155.
    • (1995) Eur. J. Obstet. Gynecol. Reprod. Biol. , vol.58 , pp. 153-155
    • Gonen, R.1    Dar, H.2    Degani, S.3
  • 6
    • 0025373291 scopus 로고
    • Multiple congenital anomalies associated with a 47,XXX chromosome constitution
    • HOOD O.J., HARTWELL E.A., SHATTUCK K.E., ROSENBERG H.S.: Multiple congenital anomalies associated with a 47,XXX chromosome constitution. Am. J. Med. Genet., 1990, 36, 73-75.
    • (1990) Am. J. Med. Genet. , vol.36 , pp. 73-75
    • Hood, O.J.1    Hartwell, E.A.2    Shattuck, K.E.3    Rosenberg, H.S.4
  • 8
    • 0343925751 scopus 로고
    • The triple X syndrome: Clinical pathological and chromosomal studies in three mentally retarded cases
    • JOHNSTON A.W., FERGUSON-SMITH M.A., HANDMAKER S.D., JONES H.V., JONES G.S.: The triple X syndrome: Clinical pathological and chromosomal studies in three mentally retarded cases. Br. Med. J., 1961, Oct. 21, 1046-1052.
    • (1961) Br. Med. J. , vol.OCT. 21 , pp. 1046-1052
    • Johnston, A.W.1    Ferguson-Smith, M.A.2    Handmaker, S.D.3    Jones, H.V.4    Jones, G.S.5
  • 9
    • 0027450295 scopus 로고
    • Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients
    • LIN H.J., NDIFORCHU F., PATELL S.: Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients. Am. J. Med. Genet., 1993, 45, 761-763.
    • (1993) Am. J. Med. Genet. , vol.45 , pp. 761-763
    • Lin, H.J.1    Ndiforchu, F.2    Patell, S.3
  • 11
    • 0027598472 scopus 로고
    • Triple-X syndrome accompanied by single maxillary central incisor: Case report
    • MIURA M., KATO N, KOJIMA H, OGUCHI H.: Triple-X syndrome accompanied by single maxillary central incisor: case report. Pediatr. Dent., 1993, 15, 214-217.
    • (1993) Pediatr. Dent. , vol.15 , pp. 214-217
    • Miura, M.1    Kato, N.2    Kojima, H.3    Oguchi, H.4
  • 13
    • 0018888964 scopus 로고
    • Language and cognitive development in 47,XXX females followed since birth
    • PENNINGTON B., PUCK M., ROBINSON A.: Language and cognitive development in 47,XXX females followed since birth. Behav.Genet., 1980, 10, 31-41.
    • (1980) Behav.Genet. , vol.10 , pp. 31-41
    • Pennington, B.1    Puck, M.2    Robinson, A.3
  • 14
    • 0023923808 scopus 로고
    • 47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation
    • SPEAR G.S., PORTO M.: 47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation. Am. J. Med. Genet., 1988, 29, 511-515.
    • (1988) Am. J. Med. Genet. , vol.29 , pp. 511-515
    • Spear, G.S.1    Porto, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.