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Journal of Clinical Pathology
Volumn 58, Issue 6, 2005, Pages 655-657
Di-George syndrome presenting with hypocalcaemia in adulthood: Two case reports and a review
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; ADULT DISEASE; BLOOD EXAMINATION; CASE REPORT; CONGENITAL HEART DISEASE; DIGEORGE SYNDROME; FAMILY PLANNING; FEMALE; GRAND MAL SEIZURE; HEALTH CARE PLANNING; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; NEWBORN DEATH; POSTMENOPAUSE; PRIORITY JOURNAL; REVIEW;
EID: 20444468958     PISSN: 00219746     EISSN: None     Source Type: Journal    
DOI: 10.1136/jcp.2004.023218     Document Type: Review
Times cited : (29)
References (10)
  • 1
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    • DiGeorge AM. Discussion of paper by Cooper MD, Peterson RDA and Good RA: a new concept of the cellular base of immunology. J Pediatr 1905;67:907.
    • (1905) J Pediatr , vol.67 , pp. 907
    • DiGeorge, A.M.1
  • 2
    • 0015421049 scopus 로고
    • DiGeorge syndrome(s)
    • Lischner HW. DiGeorge syndrome(s). J Pediatr 1972;81:1042.
    • (1972) J Pediatr , vol.81 , pp. 1042
    • Lischner, H.W.1
  • 3
    • 16944364802 scopus 로고    scopus 로고
    • Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
    • Ryan AK, Goodship JA, Wilson DI. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 1997;34:798-804.
    • (1997) J Med Genet , vol.34 , pp. 798-804
    • Ryan, A.K.1    Goodship, J.A.2    Wilson, D.I.3
  • 4
    • 0021360491 scopus 로고
    • Prevalence of T-abnormalities in infants with congenital heart disease
    • Kiel EA, Drummond WH, Barrett DJ. Prevalence of T-abnormalities in infants with congenital heart disease. Am J Dis Child 1984;138:143.
    • (1984) Am J Dis Child , vol.138 , pp. 143
    • Kiel, E.A.1    Drummond, W.H.2    Barrett, D.J.3
  • 5
    • 0027461868 scopus 로고
    • Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization
    • Desmaze C, Scambler P, Prieur M. Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization. Hum Genet 1993;90:663-5.
    • (1993) Hum Genet , vol.90 , pp. 663-665
    • Desmaze, C.1    Scambler, P.2    Prieur, M.3
  • 6
    • 0036889598 scopus 로고    scopus 로고
    • Chromosome 22q11 deletion syndrome
    • Perez E, Sullivan K. Chromosome 22q11 deletion syndrome. Curr Opin Pediatr, 2002;14:678-83.
    • (2002) Curr Opin Pediatr , vol.14 , pp. 678-683
    • Perez, E.1    Sullivan, K.2
  • 7
    • 0028473779 scopus 로고
    • Partial DiGeorge syndrome at the age of thirty-four
    • Atsushi H, Shigeto M, Eio K, et al. Partial DiGeorge syndrome at the age of thirty-four. Intern Med 1994;33:418-21.
    • (1994) Intern Med , vol.33 , pp. 418-421
    • Atsushi, H.1    Shigeto, M.2    Eio, K.3
  • 8
    • 0019937143 scopus 로고
    • The DiGeorge syndrome and the fetal alcohol syndrome
    • Ammann AJ, Wara DW, Cowan MJ. The DiGeorge syndrome and the fetal alcohol syndrome. Am J Dis Child 1982;136:900-8.
    • (1982) Am J Dis Child , vol.136 , pp. 900-908
    • Ammann, A.J.1    Wara, D.W.2    Cowan, M.J.3
  • 10
    • 0024810034 scopus 로고
    • Facial dysmorphia, parathyroid and thymic dysfunction in the father of a newborn with the DiGeorge complex
    • Maaswinkel-Mooij PD, Papapoulos SE, Gerritsen EJ, et al. Facial dysmorphia, parathyroid and thymic dysfunction in the father of a newborn with the DiGeorge complex. Eur J Pediatr 1989;149:179-83.
    • (1989) Eur J Pediatr , vol.149 , pp. 179-183
    • Maaswinkel-Mooij, P.D.1    Papapoulos, S.E.2    Gerritsen, E.J.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.