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Results: 6

Authors: TOTHFEJEL S GUNTER K MCMILIN K REIFSTECK C CHEN XN KORENBERG JR QUAN F OLSON SB MAGENIS RE
Citation: S. Tothfejel et al., HIGH-RATE OF CHROMOSOME-11 STRUCTURAL MOSAICISM IN CHROMOSOME-11 TERMINAL DELETIONS - FRAGILE SITE EXPRESSION AND CGG REPEAT EXPANSION AT FRA11B AS A GENETIC MECHANISM, American journal of human genetics, 61(4), 1997, pp. 30-30

Authors: QUAN F JANAS J TOTHFEJEL S JOHNSON DB WOLFORD JK POPOVICH BW
Citation: F. Quan et al., UNIPARENTAL DISOMY OF THE ENTIRE X-CHROMOSOME IN A FEMALE WITH DUCHENNE MUSCULAR-DYSTROPHY, American journal of human genetics, 60(1), 1997, pp. 160-165

Authors: MAGENIS RE TOTHFEJEL S OLSON S GUNTER K
Citation: Re. Magenis et al., OREGON-HEALTH-SCIENCES-UNIVERSITY STUDY - CORRELATION OF CLINICAL-DIAGNOSIS OF PRADER-WILLI AND ANGELMAN SYNDROMES AND LABORATORY TEST-RESULTS, American journal of human genetics, 57(4), 1995, pp. 670-670

Authors: TOTHFEJEL S OLSON S DURHAM C REISS J MAGENIS RE
Citation: S. Tothfejel et al., FAMILIAL MATERNAL DELETION OF D15S113 WITH BIPARENTAL METHYLATION IMPRINT OF SNRPN IN 2 HALF-SIBLING WITH ANGELMAN-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 783-783

Authors: OLSON SB TOTHFEJEL S POPOVICH B OSBORN C LAWCE H QUAN F MAGENIS E
Citation: Sb. Olson et al., FALSE-POSITIVE MALE DIAGNOSIS BY PCR AMPLIFICATION OF DYZ1 REPETITIVESEQUENCES IN FEMALE FETUS WITH LARGE CHROMOSOME-15 SATELLITE SUGGESTSCAUTION IN CHOOSING PROBES FOR ROUTINE SEXING, American journal of human genetics, 57(4), 1995, pp. 1663-1663

Authors: GRANDY DK GUNTER K HAGEN S ZHU ZW TOTHFEJEL S ZHOU QY OLSON S MAGENIS RE
Citation: Dk. Grandy et al., GENOMIC ANALYSIS OF THE HUMAN KAPPA-OPIOID RECEPTOR - NO EVIDENCE FORMULTIPLE GENES, American journal of human genetics, 57(4), 1995, pp. 1982-1982
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