transferrin has been researched along with Autosomal Chromosome Disorders in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| MANN, JD; VALDMANIS, A; VANDYKE, HE | 1 |
| BREIBART, S; EBERLEIN, WR; MELLMAN, WJ | 1 |
| Graudal, N; Milman, N; Nielsen, LS; Sørensen, SA | 1 |
| Atkins, L; Hazard, GW; Ouellette, EM; Pant, SS | 1 |
4 other study(ies) available for transferrin and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
Topics: 17-Ketosteroids; Adolescent; Adrenal Cortex Hormones; Arm; Blood Group Antigens; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 18; Estrogens; Gonadotropins; Gonadotropins, Pituitary; Haptoglobins; Humans; Intellectual Disability; Transferrin; Urine | 1964 |
DEVELOPMENTAL RETARDATION ASSOCIATED WITH AN UNBALANCED 13-15/18 TRANSLOCATION.
Topics: Blood Group Antigens; Child; Chromosome Aberrations; Chromosome Disorders; Cryptorchidism; Dermatoglyphics; Erythrocytes; Foot; Hand; Haptoglobins; Humans; Hypospadias; Intellectual Disability; Male; Seizures; Skin; Transferrin | 1964 |
HLA determinants in idiopathic haemochromatosis.
Topics: Adult; Aged; Chromosome Aberrations; Chromosome Disorders; Female; Ferritins; Genes, Recessive; Genetic Carrier Screening; Genotype; Hemochromatosis; HLA Antigens; Humans; Iron; Male; Middle Aged; Pedigree; Transferrin | 1985 |
Two cases with a C-group ring autosome.
Topics: Blood Group Antigens; Body Height; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Culture Techniques; Fibroblasts; Haptoglobins; Humans; Intellectual Disability; Karyotyping; Leukocytes; Male; Microcephaly; Movement Disorders; Muscles; Transferrin | 1966 |