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Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH
Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11)
Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader–Willi and Angelman syndrome
Unbalanced translocation t(15;22) in ‘severe’ Prader–Willi syndrome
Abnormal dicentric chromosome with co-amplification of sequences from chromosomes 11 and 19: a novel rearrangement in a patient with myelodysplastic syndrome transforming to acute
Frequency of Trisomy 15 and Loss of the Y Chromosome in Adult Leukemia
FOLLOW-UP OF CASE OF ADVANCED SURVIVAL AND TRISOMY 18
ANEUPLOIDY IN CULTURE
DERMATOGLYPHIC ANALYSES OF 32 PARENTS OF PRADER-WILLI SYNDROME INDIVIDUALS
DERMATOGLYPHIC ANALYSES OF 24 INDIVIDUALS WITH THE PRADER-WILLI SYNDROME
TRISOMY 18 IN AN 11 YEAR OLD GIRL
A Possible Genetic Variant of Homozygous Cystinuria
Diagnostic Testing for Prader-Willi and Angelman Syndromes: Response
Cytogenetic findings in cell lines derived from four ovarian carcinomas