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Clinical Application of Molecular Cytogenetics

Lee WB

  • KMID: 2104248
  • J Korean Pediatr Soc.
  • 1996 Apr;39(4):455-460.
No abstract available.
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A case of Holoprosencephaly

Lee WC, Kim IC, Lee KM, Jung CZ, LEe WB

  • KMID: 1682717
  • J Korean Pediatr Soc.
  • 1988 Dec;31(12):1674-1679.
No abstract available.
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Pulmonary Infiltration in Rotaviral Gastroenteritis

Kwak WS, Lee WB, Kim HM, Koo JH

  • KMID: 1676216
  • J Korean Pediatr Soc.
  • 1985 May;28(5):448-454.
No abstract available.
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A study on the hepatic granulocytopoiesis in human fetal liver

Hong JS, Kim KY, Lee WB, Kim DC

  • KMID: 1686685
  • Korean J Anat.
  • 1992 Dec;25(4):330-340.
No abstract available.
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Light and electron microscopic studies on the activity and the differentiation of the hepatic hemopoietic cells in fetal rat livers

Kim KY, Lee WB, Kim DC

  • KMID: 1686834
  • Korean J Anat.
  • 1991 Mar;24(1):138-152.
No abstract available.
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Noninvasive Assessment of Pressure Gradient by Quantitative Two-Dimensional Echocardiographic Doppler Studies in Pediatric Cardiovascular Diseases

Lee WB, Chung HL, Lee DJ, Lee SB

  • KMID: 1676987
  • J Korean Pediatr Soc.
  • 1987 May;30(5):518-526.
No abstract available.
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A study on variation of the origin of the deep brachial artery inKorean females.

Eum HY, Kim KY, Lee WB, Kim DC

  • KMID: 1698789
  • Korean J Phys Anthropol.
  • 1991 Jun;4(1):7-13.
No abstract available.
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Anatomic variations of insertion of the extensor pollicis brevis inKorean.

Lee MS, Chung IH, Lee HY, Chung JW, Kang HS, Ko JS, Lee WB, Park SS, Lee HS

  • KMID: 1698784
  • Korean J Phys Anthropol.
  • 1991 Dec;4(2):119-126.
No abstract available.
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Ultrastructural changes in endothelium by in-situ perfusion of hyperosmolar mannitol solution into rat brain

Erm SK, Kim KY, Lee WB, Kim DC

  • KMID: 1686604
  • Korean J Anat.
  • 1993 Dec;26(4):416-427.
No abstract available.
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A Card of Arthrogryposis Multiplex Congenita with Congenital Hypertropic Pyloric Stenosis

Yang SC, Kim SY, Kim HH, Han SH, Byun JI, Lee WB

  • KMID: 2208297
  • J Korean Pediatr Soc.
  • 1995 Nov;38(11):1577-1582.
No abstract available.
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A case of unilateral absence of pulmonary artery

Bang JH, Kim SN, Byun JI, Lee WB, Lee BC, Lee KS, Cho SH

  • KMID: 1691173
  • J Korean Pediatr Soc.
  • 1992 Jun;35(6):873-878.
No abstract available.
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Two cases of hemimegalencephaly

Yang HS, Jo B, Han SH, Byun JI, Lee WB, Lee BC, Cho SH, Yang IK

  • KMID: 1690816
  • J Korean Pediatr Soc.
  • 1992 Nov;35(11):1584-1589.
No abstract available.
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Light and electron microscopic study on dendrotoxic effect of kainic acid in hippocampus of rat brain

Choi JY, Kim KY, Lee WB, Kim DC

  • KMID: 1686603
  • Korean J Anat.
  • 1993 Dec;26(4):401-415.
No abstract available.
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A Case of Unusual (1q;21q) Translocation Down Syndrome Inherited from a t (1q;21q) Balanced Carrier Mother

Yi DH, Park JO, Shin SM, Lee YK, Kim WB, Lee WB, Park SS, Cho HI

  • KMID: 2335278
  • J Korean Pediatr Soc.
  • 1997 Aug;40(8):1156-1161.
Down syndrome is the most common autosomal syndrome in man. The incidence of trisomy 21 due to translocation is about 3.5-5%. Translocations are usually centric fusions between a 21 and...
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The relation of the median nerve to the pronator teres muscle in Koreans.

Kang HS, Cho BP, Yang YC, Cho SS, Chung IH, Ko JS, Chun MH, Lee MS, Lee WB, Park SS

  • KMID: 1698782
  • Korean J Phys Anthropol.
  • 1991 Dec;4(2):105-109.
No abstract available.
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The structural change of rat cerebral cortex by the in situ perfusion with L-glutamate, glycine and kynurenate

Kim KY, Lee WB, Kim DC

  • KMID: 1686693
  • Korean J Anat.
  • 1992 Dec;25(4):418-429.
No abstract available.
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Topographical study on the relationship of the sciatic nerve to thepiriformis muscle in Koreans.

Cho SS, Cho KJ, Lee KH, Lee WJ, Lee WB, Chung IH, Suh YS, Kang HS, Lee MS, Chung JW, Ko JS, Park SS

  • KMID: 1698790
  • Korean J Phys Anthropol.
  • 1991 Jun;4(1):15-20.
No abstract available.
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A Case of Coats' Disease

Kim YT, Lee TS, Rhee ST, Lee WB

  • KMID: 1948543
  • J Korean Ophthalmol Soc.
  • 1972 Dec;13(4):270-274.
A case of Coats' disease in 15 years old boy was presented with some clinical observation. This is a rare unilateral retinal disorder with hemorrhagic and exudative properties affecting otherwise...
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The factors on the development of coronary arterial involvement in Kawasaki disease

Kim SY, Kim JH, Byun JI, Lee WB, Lee BC, Whang KT, Lee KS, Cho SH

  • KMID: 1690849
  • J Korean Pediatr Soc.
  • 1992 Oct;35(10):1328-1335.
No abstract available.
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A Case of Rhizomelic Chondrodysplasia Punctata

Lee YD, Song MY, Kim HH, Han SH, Lee WB

  • KMID: 2335134
  • J Korean Pediatr Soc.
  • 1994 Sep;37(9):1312-1316.
Chondrodysplasia punctata is a rare congenital disorder of bone, occuring in infants, which is characterized by radiographic manifestation of premature deposition of punctate calcific densitiy in epiphyseal areas, preformed in...
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