Analysis of the Born in Bradford birth cohort

The Lancet

Volumn 383, Issue 9912, 2014, Pages 123-

  Makrythanasis, Periklis ^a   Hamamy, Hanan ^a   Antonarakis, Stylianos E ^a   Mauron, Alex ^b   Hurst, Samia A ^b  

^a Department of Genetic Medicine and Development ^*  (Switzerland)

^b UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CONGENITAL MALFORMATION; CONSANGUINITY; FAMILY PLANNING; GENETIC COUNSELING; GENETIC SCREENING; GENETIC VARIABILITY; HEMOGLOBINOPATHY; HETEROZYGOTE; HUMAN; LETTER; PRIORITY JOURNAL; CONGENITAL DISORDER; ETHNOLOGY; FEMALE; NOTE; GENETIC DISORDER; PREGNANCY; PREVALENCE; WHOLE EXOME SEQUENCING;

CONGENITAL ABNORMALITIES; FEMALE; HUMANS;

EID: 84892162381     PISSN: 01406736     EISSN: 1474547X     Source Type: Journal    
DOI: 10.1016/S0140-6736(14)60019-2     Document Type: Letter

References (5)

1. Sheridan E, Wright J, Small N, et al. Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study. Lancet 2013; 382: 1350-59.
2. Bittles AH. Consanguineous marriages and congenital anomalies. Lancet 2013; 382: 1316-17.
3. Angastiniotis MA, Hadjiminas MG. Prevention of thalassaemia in Cyprus. Lancet 1981; 317: 369-71.
4. Hamamy HA, Al-Allawi NA. Epidemiological profi le of common haemoglobinopathies in Arab countries. J Community Genet 2013; 4: 147-67.
5. Wikler D. Can we learn from eugenics?J Med Ethics 1999; 25: 183-94.