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Citation: A. Mboyo et al., Internal drainage into an Onlay-Roux-en-Y jejunal loop in isolated pancreatic injury with ductal transection: Short-term and long-term follow-up in two pediatric cases, EUR J PED S, 10(6), 2000, pp. 398-401
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Stuch, O
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Citation: O. Stuch et al., Coincidence recoil-distance Doppler-shift lifetime measurements in Ba-129,Ba-130 with EUROBALL Ge cluster detectors - art. no. 044325, PHYS REV C, 6104(4), 2000, pp. 4325
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Citation: Md. Iseman et al., Panel discussion III, INT J TUBE, 3(11), 1999, pp. S381-S387
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Weil, D
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Citation: M. Mustapha et al., An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21, HUM MOL GEN, 8(3), 1999, pp. 409-412
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Marlin, S
Weil, D
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Citation: F. Denoyelle et al., Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling, LANCET, 353(9161), 1999, pp. 1298-1303
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Kalinski, H
Weil, D
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Citation: A. Adato et al., Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance, AM J HU GEN, 65(1), 1999, pp. 261-265
Authors:
Mustapha, M
Salem, N
Weil, D
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Citation: M. Mustapha et al., Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness, EUR J HUM G, 6(6), 1998, pp. 548-551
Authors:
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Citation: Jl. Mandel et al., Physical, genetic and functional map of Xp22 - and application to identification of disease genes, BIOM HLTH R, 23, 1998, pp. 182-185