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All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders

Blood, 1997-07, Vol.90 (2), p.535-541

1997

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Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

American journal of human genetics, 1989-08, Vol.45 (2), p.193-205

1989

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Transient therapy-related myelodysplastic syndrome associated with monosomy 7 and 11q23 translocation

Leukemia, 1997-03, Vol.11 (3), p.448-450

1997

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Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation

Journal of medical genetics, 1996-11, Vol.33 (11), p.906-911

1996

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Paternal uniparental disomy of chromosome 15 in a child with angelman syndrome

Annals of neurology, 1992-10, Vol.32 (4), p.512-518

1992

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An atypical Turner syndrome patient with ring X chromosome mosaicism

Annals of clinical and laboratory science, 1995, Vol.25 (1), p.60-65

1995

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The Human Palmitoyl-CoA Ligase (FACL2) Gene Maps to the Chromosome 4q34-q35 Region by Fluorescence in Situ Hybridization (FISH) and Somatic Cell Hybrid Panels

Genomics (San Diego, Calif.), 1995-08, Vol.28 (3), p.600-602

1995

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Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes

American journal of human genetics, 1988-12, Vol.43 (6), p.948-953

1988

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Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity

American journal of human genetics, 1985-09, Vol.37 (5), p.947-955

1985

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Incidence of 15q deletions in the Angelman syndrome: A survey of twelve affected persons

American journal of medical genetics, 1989-03, Vol.32 (3), p.339-345

1989

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Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21

Genomics (San Diego, Calif.), 1989-08, Vol.5 (2), p.325-331

1989

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Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation

Clinical genetics, 1989-09, Vol.36 (3), p.189-195

1989

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Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting

American journal of medical genetics, 1990-03, Vol.35 (3), p.350-353

1990

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Localization of chromosomal DNA sequences homologous to ribosomal gene type I insertion DNA in Drosophila melanogaster

Molecular & general genetics, 1984-01, Vol.196 (2), p.345-349

1984

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Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Leukemia, 2009-02, Vol.23 (2), p.323-331

2009

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Angelman syndrome in a daughter with del(15) (q11q13) associated with brachycephaly, hearing loss, enlarged foramen magnum, and ataxia in the mother

American journal of medical genetics, 1989-03, Vol.32 (3), p.333-338

1989

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Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype

American journal of medical genetics, 1990, Vol.37 (S7), p.110-114

1990

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Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with α-satellite DNA probes: Detection of a centromeric DNA break?

American journal of medical genetics, 1992-10, Vol.44 (3), p.340-344

1992

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Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

American journal of medical genetics, 1989-05, Vol.33 (1), p.78-87

1989

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Mosaic vs. nonmosaic trisomy 9: Report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature

American journal of medical genetics, 1996-04, Vol.62 (4), p.330-335

1996

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meXicana Fashions: Politics, Self-Adornment, and Identity Construction

1, 2020

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Cytogenetic survey for autistic fragile X carriers in a mental retardation center

American journal of mental retardation, 1990-01, Vol.94 (4), p.442

1990

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Fragile (X) expression: relationship to the cell cycle

Human genetics, 1984-01, Vol.67 (1), p.99-102

1984

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Establishment of a cytogenetic service for chorionic villus samples: The split specimen approach

Prenatal diagnosis, 1990-02, Vol.10 (2), p.137-139

1990

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Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha -satellite DNA probes: Detection of a centromeric DNA break?

American journal of human genetics, 1992-01, Vol.44 (3), p.340-344

1992

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All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

Transient therapy-related myelodysplastic syndrome associated with monosomy 7 and 11q23 translocation

Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation

Paternal uniparental disomy of chromosome 15 in a child with angelman syndrome

An atypical Turner syndrome patient with ring X chromosome mosaicism

The Human Palmitoyl-CoA Ligase (FACL2) Gene Maps to the Chromosome 4q34-q35 Region by Fluorescence in Situ Hybridization (FISH) and Somatic Cell Hybrid Panels

Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes

Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity

Incidence of 15q deletions in the Angelman syndrome: A survey of twelve affected persons

Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21

Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting

Localization of chromosomal DNA sequences homologous to ribosomal gene type I insertion DNA in Drosophila melanogaster

Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Angelman syndrome in a daughter with del(15) (q11q13) associated with brachycephaly, hearing loss, enlarged foramen magnum, and ataxia in the mother

Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype

Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with α-satellite DNA probes: Detection of a centromeric DNA break?

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

Mosaic vs. nonmosaic trisomy 9: Report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature

meXicana Fashions: Politics, Self-Adornment, and Identity Construction

Cytogenetic survey for autistic fragile X carriers in a mental retardation center

Fragile (X) expression: relationship to the cell cycle

Establishment of a cytogenetic service for chorionic villus samples: The split specimen approach

Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha -satellite DNA probes: Detection of a centromeric DNA break?

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