Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Louis M. Kunkel, Kirby D. Smith, Samuel H. Boyer, +6

Proceedings of the National Academy of Sciences

Chromosome VariantsGenetic TestingCytogeneticsGenetic DisorderGenetics +11

Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

Bruce T. Lahn, Nancy Ma, W. Roy Breg, +3

Nature Genetics

Developmental BiologyMendelian DisorderRetarded MalesGenetic DisorderGenetics +5

Regional location of α1-antichymotrypsin and α1-antitrypsin genes on human chromosome 14

Mark Rabin, Michael S. Watson, Vincent J. Kidd, +3

Somatic Cell and Molecular Genetics

ChromatinCytogeneticsRegional LocationGeneticsMolecular Biology +5

Fetal blood sampling and cytogenetic abnormalities

Jui‐Der Liou, Chih‐Ping Chen, W. Roy Breg, +3

Prenatal Diagnosis

A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism

Rhea Paul, Elizabeth Dykens, James F. Leckman, +3

Journal of Autism and Developmental Disorders

Intellectual ImpairmentFragile X SyndromeDevelopmental DisabilityLanguage CharacteristicsDisability +8

Non-Random Distribution of Chromosomes in Metaphase Figures from Cultured Human Leucocytes. II. The Peripheral Location of Chromosomes 13, 17–18 and 21

O. J. Miller, W. Roy Breg, Barid B. Mukherjee, +2

Cytogenetic and Genome Research

CytogeneticsGeneticsY ChromosomeKaryotype ImagingSpectral Karyotyping +15

Tandem dup(1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies

B. Rafael Elejalde, John M. Opitz, Maria Mercedes de Elejalde, +6

American Journal of Medical Genetics

CytogeneticsGeneticsGynecologyMolecular GeneticsEmbryology +18

Regulation of rRNA gene expression in a human familial 14p+ marker chromosome

Dorothy A. Miller, W. Roy Breg, Dorothy Warburton, +2

Human Genetics

ChromatinRrna Gene ExpressionDevelopmental BiologyHuman Familial 14P+Marker Chromosome +6

Partial deletion of the short arm of chromosome No. 4(4p-): Clinical studies in five unrelated patients

Orlando J. Miller, W. Roy Breg, Dorothy Warburton, +7

The Journal of Pediatrics

Chromosome NoChromatinShort ArmCytogeneticsPartial Deletion +9

<i>NRAS </i>transforming gene maps to region p11→p13 on chromosome 1 by in situ hybridization

Mark Rabin, M. Watson, P E Barker, +3

Cytogenetic and Genome Research