메뉴 건너뛰기




Volumn 52, Issue 4, 2009, Pages 247-249

Frank-ter Haar syndrome with unusual clinical features

Author keywords

Adducted thumb; Atrial septal defect; Double outlet right ventricle; Frank ter Haar syndrome; Hypertelorism; Skeletal dysplasia

Indexed keywords

HYPERTONIC SOLUTION;

EID: 67650588814     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.03.005     Document Type: Article
Times cited : (9)

References (12)
  • 2
    • 0026599104 scopus 로고
    • Bowen syndrome: congenital glaucoma, flexion contracture of fingers and facial dysmorphism without peroxisomal abnormalities
    • Billette de Villemeur T., Bijaoui G., Beauvais P., and Richardet J.M. Bowen syndrome: congenital glaucoma, flexion contracture of fingers and facial dysmorphism without peroxisomal abnormalities. Eur. J. Pediatr. 151 (1992) 146-147
    • (1992) Eur. J. Pediatr. , vol.151 , pp. 146-147
    • Billette de Villemeur, T.1    Bijaoui, G.2    Beauvais, P.3    Richardet, J.M.4
  • 5
    • 0020351155 scopus 로고
    • Letter to the Editor: X-linked or autosomal dominant, lethal in the male: inheritance of Melnick-Needles syndrome
    • Gorlin R.J., and Knier J. Letter to the Editor: X-linked or autosomal dominant, lethal in the male: inheritance of Melnick-Needles syndrome. Am. J. Med. Genet. 13 (1982) 465-467
    • (1982) Am. J. Med. Genet. , vol.13 , pp. 465-467
    • Gorlin, R.J.1    Knier, J.2
  • 6
    • 0028932497 scopus 로고
    • Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report
    • Hamel B.C., Draaisma J.M., Pinckers A.J., Boetes C., Hoppe R.L., Ropers H.H., and Brunner H.G. Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report. Am. J. Med. Genet. 56 (1995) 312-316
    • (1995) Am. J. Med. Genet. , vol.56 , pp. 312-316
    • Hamel, B.C.1    Draaisma, J.M.2    Pinckers, A.J.3    Boetes, C.4    Hoppe, R.L.5    Ropers, H.H.6    Brunner, H.G.7
  • 9
    • 0030716477 scopus 로고    scopus 로고
    • Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family
    • Megarbane A., Tomey K., and Wakim G. Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family. Am. J. Med. Genet. 73 (1997) 67-71
    • (1997) Am. J. Med. Genet. , vol.73 , pp. 67-71
    • Megarbane, A.1    Tomey, K.2    Wakim, G.3
  • 10
    • 0029999708 scopus 로고    scopus 로고
    • Serpentine fibula syndrome: expansion of the phenotype with three affected siblings
    • Rosser E.M., Mann N.P., Hall C.M., and Winter R.M. Serpentine fibula syndrome: expansion of the phenotype with three affected siblings. Clin. Dysmorphol. 5 (1996) 105-113
    • (1996) Clin. Dysmorphol. , vol.5 , pp. 105-113
    • Rosser, E.M.1    Mann, N.P.2    Hall, C.M.3    Winter, R.M.4
  • 11
    • 0020357860 scopus 로고
    • Melnick-Needles syndrome: indication for an autosomal recessive form
    • Ter Haar B., Hamel B., Hendriks J., and de Jager J. Melnick-Needles syndrome: indication for an autosomal recessive form. Am. J. Med. Genet. 13 (1982) 469-477
    • (1982) Am. J. Med. Genet. , vol.13 , pp. 469-477
    • Ter Haar, B.1    Hamel, B.2    Hendriks, J.3    de Jager, J.4
  • 12
    • 0030963306 scopus 로고    scopus 로고
    • Extended survival in a new case of ter Haar syndrome: further delineation of the syndrome
    • Wallerstein R., Scott Jr. C.I., and Nicholson L. Extended survival in a new case of ter Haar syndrome: further delineation of the syndrome. Am. J. Med. Genet. 70 (1997) 267-272
    • (1997) Am. J. Med. Genet. , vol.70 , pp. 267-272
    • Wallerstein, R.1    Scott Jr., C.I.2    Nicholson, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.