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Citation: Sh. Park et al., CONGENITAL OLIVOPONTOCEREBELLAR ATROPHY - REPORT OF 2 SIBLINGS WITH PALEOCEREBELLAR AND NEOCEREBELLAR ATROPHY, Acta Neuropathologica, 96(4), 1998, pp. 315-321
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Citation: Lyf. Hsu et al., INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS- A COLLABORATIVE STUDY, Prenatal diagnosis, 16(1), 1996, pp. 1-28
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Citation: Ll. Estabrooks et al., PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME 4P16 BASED ON 4P DELETIONS, American journal of medical genetics, 57(4), 1995, pp. 581-586
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Citation: Lyf. Hsu et al., INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED THROUGH AMNIOCENTESIS - A COLLABORATIVE STUDY, American journal of human genetics, 57(4), 1995, pp. 259-259
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MATSUMOTO M
MILLER W
Citation: Bf. Crandall et al., MATERNAL SERUM SCREENING FOR ALPHA-FETOPROTEIN, UNCONJUGATED ESTRIOL,AND HUMAN CHORIONIC-GONADOTROPIN BETWEEN 11 AND 15 WEEKS OF PREGNANCYTO DETECT FETAL CHROMOSOME-ABNORMALITIES, American journal of obstetrics and gynecology, 168(6), 1993, pp. 1864-1869
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DUNKESCHETTER C
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Citation: Ma. Fox et al., CONSENT TO CYSTIC-FIBROSIS CARRIER SCREENING IN AN ETHNICALLY DIVERSEPOPULATION, American journal of human genetics, 53(3), 1993, pp. 50-50
Citation: Bf. Crandall et al., A GIRL WITH AN INVERTED DUPLICATED XQ AND AN ABNORMAL PHENOTYPE, American journal of human genetics, 53(3), 1993, pp. 539-539