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Acquired pericentric inversion of chromosome 9 in acute myeloid leukemia.

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Contamination of smears with "sergentella spiroides".

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Recrudescent typhus: fluctuations in titers of complement-fixing and microagglutinating antibodies to rickettsia prowazeki in persons with a history of epidemic typhus.

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BASE-STEP: A transportable antiproton reservoir for fundamental interaction studies.

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.

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Dopamine agonist-associated fibrosis in prolactinomas: clinical challenges, impacts on the tumor microenvironment, and future directions.

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