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Volume 15 Supplement 1 June 2007 ww
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Table of Contents Spoken Presentati
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Plenary Lectures Plenary Lectures P
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Plenary Lectures labile iron can be
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Concurrent Symposia S07. Vertebrate
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Concurrent Symposia S17. Towards a
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Concurrent Symposia 11 at E13.5 sim
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Concurrent Symposia 1 phomagenesis.
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cover cryptic mutations in Drosophi
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Concurrent Sessions first excluded
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Concurrent Sessions of 210 ancestry
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Concurrent Sessions C23. Literature
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Concurrent Sessions a boy with a ty
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Concurrent Sessions C40. Mutation o
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Concurrent Sessions C48. CHROMSCAN:
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Concurrent Sessions C57. RNAi-based
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Concurrent Sessions been replicated
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Concurrent Sessions involved in an
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Concurrent Sessions tion considers
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Clinical genetics lateral neurosens
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Clinical genetics apparently sporad
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Clinical genetics itar syndrome, wh
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Clinical genetics diseases, Foundat
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Clinical genetics P0041. The first
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Clinical genetics EFNB1 was found t
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Clinical genetics of the CSB gene.
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Clinical genetics growth retardatio
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Clinical genetics PCR with a modifi
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Clinical genetics pound heterozygou
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Clinical genetics plicated: two cou
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Clinical genetics P0105. APC gene m
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Clinical genetics an indication of
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Clinical genetics great importance
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Clinical genetics P0133. Hidrotic e
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Clinical genetics eight patients as
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Clinical genetics P0152. Kabuki syn
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Clinical genetics P0161. Intrafamil
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Clinical genetics matter and normal
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Clinical genetics type at 550 bands
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Clinical genetics will be confirmed
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Clinical genetics nosed. Accurate r
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Clinical genetics which has not bee
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Clinical genetics P0217. Partial mo
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Clinical genetics fested progeroid
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Clinical genetics A 29 years old ma
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Clinical genetics ing loss (HHL). I
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Clinical genetics dació Son Llatze
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Clinical genetics These preliminary
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Clinical genetics P0272. Williams S
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Cytogenetics Po02. Cytogenetics P02
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Cytogenetics to reports from Saudi
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Cytogenetics P0298. Female-specific
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Cytogenetics P0306. Lipoatrophic pa
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Cytogenetics 22 leading to the form
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Cytogenetics somal sperm and that o
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Cytogenetics University of Belgrade
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Cytogenetics Within the same metaph
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Cytogenetics Less than 10 cases of
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Cytogenetics lar markers taken from
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Cytogenetics Brain Unaffected Schiz
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Cytogenetics ability with no speech
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Cytogenetics P0389. An age based cy
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Cytogenetics P0399. Molecular Chara
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Cytogenetics ing of complex examina
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Cytogenetics letion in 5q33 in all
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Cytogenetics and his son carried th
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Prenatal diagnosis tion about famil
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Prenatal diagnosis P0443. The risk
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Prenatal diagnosis in house PCR pro
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Prenatal diagnosis P0462. Increased
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Prenatal diagnosis P0471. Preimplan
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Prenatal diagnosis agreement with w
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Prenatal diagnosis of Turner Syndro
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Cancer genetics ously defined for d
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Cancer genetics Their frequencies w
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Cancer genetics tion Clinic-Portugu
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Cancer genetics tric carcinogenesis
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Cancer genetics P0532. Secondary ch
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Cancer genetics P0542. Differential
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Cancer genetics gastric cancer risk
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Cancer genetics ania, 3 The Institu
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Cancer genetics low: 8% (8/98 sampl
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Cancer genetics P0578. Somatic mito
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Cancer genetics P0587. Differential
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Cancer genetics cinoma (ESCC), whic
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Cancer genetics method to measure t
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Cancer genetics pression (compared
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Cancer genetics to available biolog
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Molecular and biochemical basis of
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Genetic analysis, linkage, and asso
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Normal variation, population geneti
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genomics, technology, bioinformatic
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Genetic counselling, education, gen
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Genetic counselling, education, gen
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Genetic counselling, education, gen
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Genetic counselling, education, gen
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Genetic counselling, education, gen
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Genetic counselling, education, gen
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- Page 347 and 348: Therapy for genetic disease Po10. T
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- Page 353 and 354: Author Index 1 Arslan-Krichner, M.:
- Page 355 and 356: Author Index Borkowska, A.: P1089 B
- Page 357 and 358: Author Index Coviello, D.: P0078, P
- Page 359 and 360: Author Index Estivill, X.: P1216, P
- Page 361 and 362: Author Index Graf, S. A.: P0021 Gra
- Page 363 and 364: Author Index 1 Josifiova, D.: PL07
- Page 365 and 366: Author Index Laurier, V.: C03 Lauri
- Page 367 and 368: Author Index Melo, D. G.: P0260, P0
- Page 369 and 370: Author Index Osorio, P.: P0218 Osta
- Page 371 and 372: Author Index Reese, T.: C06 Regal,
- Page 373 and 374: Author Index 1 Shaposhnikov, S.: P0
- Page 375 and 376: Author Index Touitou, I.: P0733 Tou
- Page 377 and 378: Author Index Xiao, C.: P1241 Xie, G
- Page 379 and 380: Keyword Index ARMR: P0907 array CGH
- Page 381 and 382: Keyword Index Consanguineous marria
- Page 383 and 384: Keyword Index 1 Fronto-temporal dem
- Page 385 and 386: Keyword Index IRF5: P1086 IRF6: P07
- Page 387 and 388: Keyword Index NBS1 gene: P0567 NBS-
- Page 389: Keyword Index P1085 Rep1: P1104 rep
- Page 393 and 394: Notes 1
- Page 395 and 396: A natural choice in Fabry Disease P
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