Detection of the X-chromatin body in human fibroblasts by quinacrine fluoromicroscopy.
Explore the source record for details and available documents.
Female↗
Biomedical subjects
F Hecht
Publications and source records attributed to F Hecht.
Chromosomal localization of the heterochromatic region 16qh(.76) linked to alpha-haptoglobin in man.
Explore the source record for details and available documents.
Analysis of Variance↗
Familial hypersensitivity to insect stings.
Explore the source record for details and available documents.
Child↗
Testosterone-binding protein probably not Y-linked.
Explore the source record for details and available documents.
Genes, Dominant↗
Family chromosome studies.
Explore the source record for details and available documents.
Abnormalities, Multiple↗
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
Explore the source record for details and available documents.
Acid Phosphatase↗
Familial predisposition to thyroid disease in Down's syndrome: controlled immunoclinical studies.
Explore the source record for details and available documents.
Adolescent↗
A mother with Down's syndrome and her chromosomally normal infant.
Explore the source record for details and available documents.
Adult↗
Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.
Explore the source record for details and available documents.
Autoradiography↗
Congenital contractural arachnodactyly. A heritable disorder of connective tissue.
Explore the source record for details and available documents.
Child↗
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.
We have found recurrent chromosome breaks at a site (the "fragile site") on the long arm of chromosome 16. This site segregates in simple Mendelian dominant fashion in a large family. The distal portion of the chromosome sometimes shows selective endoreduplication. Preliminary linkage results reveal only 3 recombinants in 33 opportunities for recombination between the fragile site and the alpha locus of haptoglobin, an indication that the alpha-Hp gene is located near this region on chromosome 16.
Adolescent↗
Meiotic evidence in Down's syndrome for 21/21 chromosome translocation or isochromosome.
Explore the source record for details and available documents.
Adolescent↗
Genetic diagnosis in the newborn. A part of preventive medicine.
Explore the source record for details and available documents.
Adolescent↗
Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome.
Explore the source record for details and available documents.
Adolescent↗
Transformation of blood lymphocytes in ataxia telangiectasia. Dose and time response to phytohemagglutinin.
Explore the source record for details and available documents.
Ataxia Telangiectasia↗
Impaired in vitro response of circulating lymphocytes to phytohemagglutinin in Down's syndrome: dose- and time-response curves and relation to cellular immunity.
Explore the source record for details and available documents.
Adult↗
Hemoglobin-Seattle (alpha-2 beta-2 76-Glu): an unstable hemoglobin causing chronic hemolytic anemia.
Explore the source record for details and available documents.
Adult↗