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
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