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Annals of human biology·2003

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The British journal of dermatology·2000

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Familial autosomal dominant dopa responsive Parkinson's disease in three living generations showing extreme anticipation and childhood onset.

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Acquired pericentric inversion of chromosome 9 in acute myeloid leukemia.

Trisomy 21 as a sole acquired abnormality in an adult Omani patient with CD7- and CD9-positive acute myeloid leukemia.

Consanguinity and genetic morbidity in a British primary care setting: a pilot study with trained linkworkers.

The clinical genetics of hidradenitis suppurativa revisited.

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.

Familial autosomal dominant dopa responsive Parkinson's disease in three living generations showing extreme anticipation and childhood onset.

Intravenous iron to treat anaemia before cardiac surgery (ITACS): international, double blind, placebo controlled randomised trial.

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Effectiveness of the BabyBreathe intervention for maintaining postpartum smoking cessation: multicentre pragmatic randomised controlled trial.

High-dose folic acid therapy ameliorates gut microbiota dysbiosis in reproductive-aged women with hyperhomocysteinemia.

First Trimester Fetal Renal Pelvis Diameter Cut-Off Values for Predicting Fetal Pelviectasis in Advanced Gestation.

Validation of Claims-Based Algorithms for Identifying Congenital Urinary Tract, Genital, Gastrointestinal, and Musculoskeletal Malformations.

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