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Chromosomal assignment of three human melanocyte-specific genes.

International journal of oncology·2011

Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion.

American journal of medical genetics. Part A·2009

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European journal of human genetics : EJHG·2008

Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.

Clinical genetics·2008

Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.

Journal of medical genetics·2008

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

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Birth defects original article series·1996

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Polish journal of radiology·2026

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Journal of the Korean Society of Radiology·2026

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Frontiers in oncology·2026

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Frontiers in oncology·2026

An integrated experimental and computational study on a COX-2-targeted AIE probe for precise cancer cell imaging via restriction of intramolecular rotation.

Analytica chimica acta·2026

Autofluorescence-Based Devices for Oral Cancer Screening - A Scoping Review.

Journal of dentistry·2026

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