[Free trisomy concerning a little acrocentric chromosome in a non-mongoloid female patient. Trisomy 22 or partial trisomy D?]. 1970

G Malpuech, and G Menut, and E J Raynaud, and A Lavignon

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014314 Trisomy The possession of a third chromosome of any one type in an otherwise diploid cell. Partial Trisomy,Chromosomal Triplication,Chromosomal Triplications,Partial Trisomies,Trisomies,Trisomies, Partial,Trisomy, Partial
D025063 Chromosome Disorders Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429) Autosomal Chromosome Disorders,Chromosome Abnormality Disorders,Chromosomal Disorders,Autosomal Chromosome Disorder,Chromosomal Disorder,Chromosome Abnormality Disorder,Chromosome Disorder,Chromosome Disorder, Autosomal,Chromosome Disorders, Autosomal,Disorder, Chromosomal,Disorder, Chromosome,Disorder, Chromosome Abnormality,Disorders, Chromosomal,Disorders, Chromosome

Related Publications

G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
September 1975, Humangenetik,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
January 1974, Clinical genetics,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
June 1983, Pediatria polska,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
June 1973, Journal of mental deficiency research,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
October 2007, American journal of medical genetics. Part A,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
November 1974, Helvetica paediatrica acta,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
December 1971, Journal of medical genetics,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
June 1962, American journal of human genetics,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
April 2006, Experimental and molecular pathology,
G Malpuech, and G Menut, and E J Raynaud, and A Lavignon
January 1968, Humangenetik,
Copied contents to your clipboard!