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Strengman, E
Weemaes, C
Pearson, PL
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Authors:
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Narayan, A
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Sohn, OS
Ehrlich, M
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Tuck-Muller, CM
Narayan, A
Tsien, F
Smeets, DFCM
Sawyer, J
Fiala, ES
Sohn, OS
Ehrlich, M
Citation: Cm. Tuck-muller et al., DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients, CYTOG C GEN, 89(1-2), 2000, pp. 121-128
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Vietor, HE
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Citation: He. Vietor et al., Immunological tolerance in an HLA non-identical chimeric twin (vol 61, pg 190, 2000), HUMAN IMMUN, 61(7), 2000, pp. 720-720
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Citation: J. Celli et al., Familial syndromic esophageal atresia maps to 2p23-p24, AM J HU GEN, 66(2), 2000, pp. 436-444
Authors:
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Hamel, BCJ
Citation: Gjcm. Van Buggenhout et al., Down syndrome in a population of elderly mentally retarded patients: Genetic-diagnostic survey and implications for medical care, AM J MED G, 85(4), 1999, pp. 376-384
Authors:
Hamel, BCJ
Smits, APT
van den Helm, B
Smeets, DFCM
Knoers, NVAM
van Roosmalen, T
Thoonen, GHJ
Assman-Hulsmans, CFCH
Ropers, HH
Mariman, ECM
Kremer, H
Citation: Bcj. Hamel et al., Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: Clinical and psychometric data and results of linkage analysis, AM J MED G, 85(3), 1999, pp. 290-304
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Yntema, HG
van den Helm, B
Knoers, NVAM
Smits, APT
van Roosmalen, T
Smeets, DFCM
Mariman, ECM
van der Burgt, I
van Bokhoven, H
Ropers, HH
Kremer, H
Hamel, BCJ
Citation: Hg. Yntema et al., X-linked mental retardation: Evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region, AM J MED G, 85(3), 1999, pp. 305-308