phosphorus has been researched along with Autosomal Chromosome Disorders in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (75.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
De La Villemarque, R; Derrien, C; Henry, C; Maugendre, D; Odent, S; Poirier, JY | 1 |
Witkop, CJ | 1 |
Fraser, D; Scriver, CR | 1 |
Garn, SM | 1 |
2 review(s) available for phosphorus and Autosomal Chromosome Disorders
Article | Year |
---|---|
Clinical aspects of dental anomalies.
Topics: Bone Diseases, Developmental; Chromosome Aberrations; Chromosome Disorders; Dental Pulp Cavity; Dentin Dysplasia; Dentinogenesis Imperfecta; Humans; Hypophosphatasia; Hypophosphatemia, Familial; Odontodysplasia; Phosphorus; Pseudohypoparathyroidism; Racial Groups; Rickets; Syndrome; Tooth Abnormalities | 1976 |
The course of bone gain and the phases of bone loss.
Topics: Adolescent; Adult; Africa; Aged; Aging; Black People; Body Height; Body Weight; Bone Development; Bone Diseases, Developmental; Bone Resorption; Calcium, Dietary; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet; Female; Humans; Income; Infant; Male; Middle Aged; Osteogenesis Imperfecta; Phosphorus; Sex Factors; Trisomy; United States; White People | 1972 |
2 other study(ies) available for phosphorus and Autosomal Chromosome Disorders
Article | Year |
---|---|
[Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation].
Topics: Abnormalities, Multiple; Adult; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 22; Diagnosis, Differential; Face; Female; Fibrous Dysplasia, Polyostotic; Humans; Hypercalcemia; Hypoparathyroidism; In Situ Hybridization, Fluorescence; Infant, Newborn; Intellectual Disability; Obesity; Parathyroid Hormone; Phenotype; Phosphorus; Pregnancy; Pregnancy Complications; Pseudohypoparathyroidism; Purpura, Thrombocytopenic, Idiopathic; Scoliosis; Syndrome; Velopharyngeal Insufficiency | 2001 |
Familial forms of vitamin D-resistant rickets revisited. X-linked hypophosphatemia and autosomal recessive vitamin D dependency.
Topics: Calcium; Chromosome Aberrations; Chromosome Disorders; Dihydroxycholecalciferols; Female; Genes, Recessive; Humans; Hydroxycholecalciferols; Hyperparathyroidism; Hypophosphatemia, Familial; Male; Phenotype; Phosphates; Phosphorus; Sex Chromosome Aberrations; Vitamin D | 1976 |