BIOMAT Database Logo BIOMAT Database Logo

Genetic studies of the Seneca Indians: haptoglobins, transferrins, G-6-PD deficiency, hemoglobinopathy, color blindness, morphological traits and dermatoglyphics. 1968

T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman

UI MeSH Term Description Entries
D007198 Indians, North American Members of indigenous North American populations with pre-colonial contact origins. Amerinds, North American,Indigenous North Americans,American Indian, North,American, Indigenous North,Amerind, North American,Indian, North American,Indigenous North American,North American Amerind,North American Amerinds,North American Indian,North American Indians,North American, Indigenous
D008297 Male Males
D009518 New York State bounded on the north by Lake Ontario and Canada, on the east by Vermont, Massachusetts, and Connecticut, on the south by the Atlantic Ocean, New Jersey, and Pennsylvania, and on the west by Pennsylvania, Lake Erie, and Canada.
D003117 Color Vision Defects Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue. Achromatopsia,Color Blindness,Monochromatopsia,Color Blindness, Acquired,Color Blindness, Blue,Color Blindness, Green,Color Blindness, Inherited,Color Blindness, Red,Color Blindness, Red-Green,Color Vision Deficiency,Deutan Defect,Protan Defect,Tritan Defect,Achromatopsias,Acquired Color Blindness,Blindness, Color,Blue Color Blindness,Color Blindness, Red Green,Color Vision Defect,Color Vision Deficiencies,Defect, Color Vision,Defect, Deutan,Defects, Color Vision,Deficiencies, Color Vision,Deficiency, Color Vision,Green Color Blindness,Inherited Color Blindness,Red Color Blindness,Red-Green Color Blindness,Vision Defect, Color,Vision Defects, Color,Vision Deficiencies, Color,Vision Deficiency, Color
D003878 Dermatoglyphics The study of the patterns of ridges of the skin of the fingers, palms, toes, and soles. Fingerprints,Plantar Prints,Fingerprint,Plantar Print,Print, Plantar,Prints, Plantar
D004431 Ear, External The outer part of the hearing system of the body. It includes the shell-like EAR AURICLE which collects sound, and the EXTERNAL EAR CANAL, the TYMPANIC MEMBRANE, and the EXTERNAL EAR CARTILAGES. External Ear,Outer Ear,Ear, Outer,Ears, External,Ears, Outer,External Ears,Outer Ears
D004586 Electrophoresis An electrochemical process in which macromolecules or colloidal particles with a net electric charge migrate in a solution under the influence of an electric current. Electrophoreses
D005260 Female Females
D005385 Fingers Four or five slender jointed digits in humans and primates, attached to each HAND. Finger
D005787 Gene Frequency The proportion of one particular in the total of all ALLELES for one genetic locus in a breeding POPULATION. Allele Frequency,Genetic Equilibrium,Equilibrium, Genetic,Allele Frequencies,Frequencies, Allele,Frequencies, Gene,Frequency, Allele,Frequency, Gene,Gene Frequencies

Related Publications

T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
[G-6-PD deficiency with hemoglobinopathy and alpha-thalassemia].
January 1968, Acta haematologica,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
Genetic implications of G-6-PD deficiency.
June 1976, The New England journal of medicine,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
Hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness.
January 1988, Japanese journal of ophthalmology,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
New genetic variants of transferrins and haptoglobins in pigs.
June 1966, Nature,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
THE COLOR-BLINDNESS OF INDIANS.
May 1930, Science (New York, N.Y.),
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
The serum haptoglobins and transferrins.
January 1962, Bibliotheca haematologica,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
[Dermatoglyphics in genetic eye diseases: retinal pigmentosa and congenital color blindness].
February 1985, Zhonghua yi xue za zhi,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
Acetamonophen and G-6-PD deficiency.
January 1984, Acta haematologica,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
G-6-PD deficiency and primaquine.
January 1983, The Journal of the Association of Physicians of India,
T D Doeblin, and G B Ingall, and P H Pinkerton, and K R Dronamraju, and R M Bannerman
Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. II. Incidence of G-6-PD deficiency in Japanese.
October 1965, Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society,
Copied contents to your clipboard!