Fetal Macrosomia
What's New
Last Posted: Apr 20, 2024
- TCF7L2 Polymorphism rs7903146 (C/T) and Gestational Diabetes Influence on Obstetric Outcome: A Romanian Case-Control Study.
Gheorghe Cruciat, et al. International journal of molecular sciences 2024 0 (7) - Association between rankl [RS9594759] and IL10 [RS1800896] Genes polymorphism and deciduous tooth eruption terms in Ukrainians born macrosomic.
Garmash Olga V, et al. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2020 0 (2) 342-351 - Individualized Supplement of Folic Acid Based on the Gene Polymorphisms of MTHER/MTRR Reduced the Incidence of Adverse Pregnancy Outcomes and Newborn Defects.
Yang J, et al. Nigerian journal of clinical practice 2021 8 (8) 1150-1158 - Fibulin-5 (FBLN5) gene polymorphism is associated with pelvic organ prolapse.
Khadzhieva Maryam B, et al. Maturitas 2014 8 (4) 287-92 - Fetal macrosomia
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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