Genetic factors contributing to birth weight

Archives of Disease in Childhood: Fetal and Neonatal Edition

Volumn 86, Issue 1, 2002, Pages

  Johnston, L B ^a   Clark, A J L ^a   Savage, M O ^a  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BIRTH WEIGHT; CHROMOSOMAL LOCALIZATION; CONFERENCE PAPER; GENETIC SUSCEPTIBILITY; GENETICS; PRIORITY JOURNAL; RISK FACTOR;

EID: 0036144995     PISSN: 13592998     EISSN: 14682052     Source Type: Journal    
DOI: 10.1136/fn.86.1.f2-a     Document Type: Conference Paper

References (21)

1. Parental determinants of birth weight
2. Causes of variation in birth weight: A study of offspring of twins
3. Some recent trends in human genetics
4. Relative effect of parental birth weight on infant birth weight at term
5. Birth weight of relatives by maternal tendency to repeat small-for-gestational-age (SGA) births in successive pregnancies
6. Familial aggregation of low birth weight among whites and blacks in the United States
7. Further evidence for a significant effect of fetal genes on variation in birth weight
8. Genetic, metabolic and clinical characteristics of maturity onset diabetes of the young
9. Mutations in the glucokinase gene of the fetus result in reduced birth weight
10. Confined placental mosaicism and intrauterine fetal growth
11. Chromosomal mosaicism confined to the placenta in human conceptions
12. Confined placental mosaicism and intrauterine growth retardation: A case-control analysis of placentas at delivery
13. Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r)
14. Role of insulin-like growth factors in embryonic and postnatal growth. Role of insulin-like growth factors in embryonic and postnatal growth
15. Insulin resistance and growth retardation in mice lacking insulin receptor substrate-1
16. Targeted gene mutations define the roles of insulin and IGF-1 receptors in mouse embryonic development
17. Intrauterine growth retardation and postnatal growth failure associated with deletion of the insulin-like growth factor I gene
18. Association of the INS VNTR with size at birth
19. Molecular studies in 37 Silver-Russell syndrome patients: Frequency and etiology of uniparental disomy
20. Maternal uniparental disomy 7 in Silver-Russell syndrome
21. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation