Imprinting moves to the centre

[1] INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15 [J]. NATURE GENETICS, 1995, 9 (04) : 395 - 400

[2] Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene [J]. NATURE GENETICS, 1996, 14 (02) : 163 - 170

[3] ELLIOT M, 1994, J MED GENET, V7, P560

[4] EMBRYOLOGICAL AND MOLECULAR INVESTIGATIONS OF PARENTAL IMPRINTING ON MOUSE CHROMOSOME-7 [J]. NATURE, 1991, 351 (6328) : 667 - 670

[5] An imprinted gene p57(KIP2) is mutated in Beckwith-Wiedemann syndrome [J]. NATURE GENETICS, 1996, 14 (02) : 171 - 173

[6] Genomic imprinting of human p57(KIP2) and its reduced expression in Wilms' tumors [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (06) : 783 - 788

[7] Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) : 12456 - 12460

[8] LOSS OF THE IMPRINTED IGF2/CATION-INDEPENDENT MANNOSE 6-PHOSPHATE RECEPTOR RESULTS IN FETAL OVERGROWTH AND PERINATAL LETHALITY [J]. GENES & DEVELOPMENT, 1994, 8 (24) : 2953 - 2963

[9] UNIPARENTAL DISOMY IN HUMANS - DEVELOPMENT OF AN IMPRINTING MAP AND ITS IMPLICATIONS FOR PRENATAL-DIAGNOSIS [J]. HUMAN MOLECULAR GENETICS, 1995, 4 : 1757 - 1764

[10] P57(KIP2), A STRUCTURALLY DISTINCT MEMBER OF THE P21(CIP1) CDK INHIBITOR FAMILY, IS A CANDIDATE TUMOR-SUPPRESSOR GENE [J]. GENES & DEVELOPMENT, 1995, 9 (06) : 650 - 662

[1] INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15 [J]. NATURE GENETICS, 1995, 9 (04) : 395 - 400

[2] Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene [J]. NATURE GENETICS, 1996, 14 (02) : 163 - 170

[3] ELLIOT M, 1994, J MED GENET, V7, P560

[4] EMBRYOLOGICAL AND MOLECULAR INVESTIGATIONS OF PARENTAL IMPRINTING ON MOUSE CHROMOSOME-7 [J]. NATURE, 1991, 351 (6328) : 667 - 670

[5] An imprinted gene p57(KIP2) is mutated in Beckwith-Wiedemann syndrome [J]. NATURE GENETICS, 1996, 14 (02) : 171 - 173

[6] Genomic imprinting of human p57(KIP2) and its reduced expression in Wilms' tumors [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (06) : 783 - 788

[7] Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) : 12456 - 12460

[8] LOSS OF THE IMPRINTED IGF2/CATION-INDEPENDENT MANNOSE 6-PHOSPHATE RECEPTOR RESULTS IN FETAL OVERGROWTH AND PERINATAL LETHALITY [J]. GENES & DEVELOPMENT, 1994, 8 (24) : 2953 - 2963

[9] UNIPARENTAL DISOMY IN HUMANS - DEVELOPMENT OF AN IMPRINTING MAP AND ITS IMPLICATIONS FOR PRENATAL-DIAGNOSIS [J]. HUMAN MOLECULAR GENETICS, 1995, 4 : 1757 - 1764

[10] P57(KIP2), A STRUCTURALLY DISTINCT MEMBER OF THE P21(CIP1) CDK INHIBITOR FAMILY, IS A CANDIDATE TUMOR-SUPPRESSOR GENE [J]. GENES & DEVELOPMENT, 1995, 9 (06) : 650 - 662