Layla N. Al-Jader

Hereditary haemochromatosis: only 1% of adult HFE C282Y homozygotes in South Wales have a clinical diagnosis of iron overload

Anne McCune, Layla N. Al-Jader, Alison May et al. · Human Genetics · 2002 · 76 citations

Heme Homeostasis, Genetic Disorder, Iron Metabolism +10

Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosis

Layla N. Al-Jader, M C Goodchild, H C Ryley et al. · Clinical Genetics · 1990 · 69 citations

Survey of attitudes of pregnant women towards Down syndrome screening

Layla N. Al-Jader, Nina Parry‐Langdon, R. J. William Smith · Prenatal Diagnosis · 2000 · 52 citations

Outbreak of Escherichia coli O157 in a nursery: lessons for prevention

Layla N. Al-Jader, R Salmon, A M Walker et al. · Archives of Disease in Childhood · 1999 · 41 citations · Full text

Frequency of carriers of cystic fibrosis gene among patients with myeloid malignancy and melanoma.

N Warren, Jordan A. Holmes, Layla N. Al-Jader et al. · BMJ · 1991 · 27 citations · Full text

Cystic Fibrosis Gene, Fibrosis, Medicine +6