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Volumn 8, Issue 2, 1999, Pages 147-150

Robinow syndrome in monozygotic twins with normal stature

Author keywords

Fetal face; Omphalocele; Robinow syndrome

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BODY HEIGHT; CASE REPORT; HUMAN; MALE; MONOZYGOTIC TWINS; NEWBORN; OMPHALOCELE; PHALANX HYPOPLASIA; PRIORITY JOURNAL; ROBINOW SYNDROME; SKELETON RADIOGRAPHY;

EID: 0032950840     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199904000-00012     Document Type: Article
Times cited : (6)

References (12)
  • 1
    • 0022443827 scopus 로고
    • Robinow syndrome without mesomelic 'brachymelia': A report of five cases
    • Bain MD, Winter RM, Burn J (1986). Robinow syndrome without mesomelic 'brachymelia': a report of five cases. J Med Genet 23:350-354.
    • (1986) J Med Genet , vol.23 , pp. 350-354
    • Bain, M.D.1    Winter, R.M.2    Burn, J.3
  • 2
    • 0018938130 scopus 로고
    • The syndromes of Marshall and Weaver
    • Fitch N (1980). The syndromes of Marshall and Weaver. J Med Genet 17:174-178.
    • (1980) J Med Genet , vol.17 , pp. 174-178
    • Fitch, N.1
  • 3
    • 0026670134 scopus 로고
    • Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature
    • Garganta CL, Bodurtha JN (1992). Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature. Am J Med Genet 44:129-135.
    • (1992) Am J Med Genet , vol.44 , pp. 129-135
    • Garganta, C.L.1    Bodurtha, J.N.2
  • 4
    • 0029894685 scopus 로고    scopus 로고
    • Síndrome de robinow: Presentación de una familia con transmisión autosómica dominante
    • López MTD, Sanz GL, Castilla AQ, Pablo CE, Meix JMA (1996). Síndrome de Robinow: presentación de una familia con transmisión autosómica dominante. An Esp Pediatr 44:520-523.
    • (1996) An Esp Pediatr , vol.44 , pp. 520-523
    • López, M.T.D.1    Sanz, G.L.2    Castilla, A.Q.3    Pablo, C.E.4    Meix, J.M.A.5
  • 6
    • 0025165804 scopus 로고
    • Concurrence of Robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins
    • Nazer H, Gunasekaran TS, Sakati NA, Nyhan WL (1990). Concurrence of Robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins. Am J Med Genet 37:516-518.
    • (1990) Am J Med Genet , vol.37 , pp. 516-518
    • Nazer, H.1    Gunasekaran, T.S.2    Sakati, N.A.3    Nyhan, W.L.4
  • 8
    • 0001798076 scopus 로고
    • Robinow syndrome
    • Buyse ML Dover: Blackwell Scientific Publications
    • Robinow M (1990). Robinow syndrome. In Buyse ML (ed): Birth Defects Encyclopedia, Dover: Blackwell Scientific Publications; pp. 1499-1500.
    • (1990) Birth Defects Encyclopedia , pp. 1499-1500
    • Robinow, M.1
  • 12
    • 0025159356 scopus 로고
    • Autosomal recessive Robinow syndrome
    • Teebi AS (1990). Autosomal recessive Robinow syndrome. Am J Med Genet 35:64-68.
    • (1990) Am J Med Genet , vol.35 , pp. 64-68
    • Teebi, A.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.