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Volumn 16, Issue 3, 2003, Pages 457-459

Congenital hypothyroidism associated with Rubinstein-Taybi syndrome

Author keywords

Congenital hypothyroidism; Newborn; Rubinstein Taybi syndrome

Indexed keywords

IODINE; LEVOTHYROXINE SODIUM; OXYGEN;

EID: 0141995475     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2003.16.3.457     Document Type: Article
Times cited : (7)

References (15)
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    • Rubinstein, J.H.1    Taybi, H.2
  • 2
    • 0141956855 scopus 로고    scopus 로고
    • Specific genetic disorders presenting in the newborn
    • Taeusch HW, Ballard RA, eds. Philadelphia, PA: WB Saunders Co
    • Shephard B, Kupke KG. Specific genetic disorders presenting in the newborn. In: Taeusch HW, Ballard RA, eds. Avery's Diseases of the Newborn. Philadelphia, PA: WB Saunders Co., 1998; 209-228.
    • (1998) Avery's Diseases of the Newborn , pp. 209-228
    • Shephard, B.1    Kupke, K.G.2
  • 3
    • 0025045983 scopus 로고
    • Broad thumb-first toe (Rubinstein-Taybi) syndrome 1957-1988
    • Rubinstein JH. Broad thumb-first toe (Rubinstein-Taybi) syndrome 1957-1988. Am J Med Genet 1990; S6: 3-16.
    • (1990) Am. J. Med. Genet. , vol.S6 , pp. 3-16
    • Rubinstein, J.H.1
  • 5
    • 0023948591 scopus 로고
    • Congenital abnormalities and congenital hypothyroidism
    • Lazarus JH, Hughes IA. Congenital abnormalities and congenital hypothyroidism. Lancet 1988; ii: 52.
    • (1988) Lancet , vol.2 , pp. 52
    • Lazarus, J.H.1    Hughes, I.A.2
  • 6
    • 0026723020 scopus 로고
    • Congenital anomalies concomitant with persistent primary congenital hypothyroidism
    • Siebner R, Merlob P, Kaiserman I, Sack J. Congenital anomalies concomitant with persistent primary congenital hypothyroidism. Am J Med Genet 1992; 44: 57-60.
    • (1992) Am. J. Med. Genet. , vol.44 , pp. 57-60
    • Siebner, R.1    Merlob, P.2    Kaiserman, I.3    Sack, J.4
  • 8
    • 0030991994 scopus 로고    scopus 로고
    • Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992
    • Roberts HE, Moore CA, Fernhoff PM, Brown AL, Khoury MJ. Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992. Am J Med Genet 1997; 71: 29-32.
    • (1997) Am. J. Med. Genet. , vol.71 , pp. 29-32
    • Roberts, H.E.1    Moore, C.A.2    Fernhoff, P.M.3    Brown, A.L.4    Khoury, M.J.5
  • 10
    • 0031662327 scopus 로고    scopus 로고
    • Colloidon baby concomitant with congenital hypothyroidism: A patient report and review of the literature
    • Kurtoǧlu S, Çaksen H, Erdoǧan R, Kisaarslan AF. Colloidon baby concomitant with congenital hypothyroidism: a patient report and review of the literature. J Pediatr Endocrinol Metab 1998; 11: 569-573.
    • (1998) J. Pediatr. Endocrinol. Metab. , vol.11 , pp. 569-573
    • Kurtoǧlu, S.1    Çaksen, H.2    Erdoǧan, R.3    Kisaarslan, A.F.4
  • 14


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.