Author Details
Erickson, RP
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Vol 45, No 1 (2012) - Articles
MASSIVELY PARALLEL DNA SEQUENCING AND THE NEW APPROACH TO MUTATION DETECTION: A STEP TOWARDS A LYMPHEDEMA FINE PANEL
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Vol 41, No 3 (2008) - Articles
NOVEL FOXC2 MISSENSE MUTATION IDENTIFIED IN PATIENT WITH LYMPHEDEMA-DISTICHIASIS SYNDROME AND REVIEW
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Vol 42, No 4 (2009) - Articles
LYMPHEDEMA-DISTICHIASIS SYNDROME WITHOUT FOXC2 MUTATION: EVIDENCE FOR CHROMOSOME 16 DUPLICATION UPSTREAM OF FOXC2
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Vol 39, No 2 (2006) - Articles
COMPARATIVE LYMPHATIC, OCULAR, AND METABOLIC PHENOTYPES OF FOXC2 HAPLOINSUFFICIENT AND AP2-FOXC2 TRANSGENIC MICE
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Vol 36, No 4 (2003) - Articles
CARDIO(BLOOD-LYMPH)VASCULAR GENOMICS: NEED FOR A TERMINOLOGY ADJUSTMENT
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Vol 34, No 1 (2001) - Articles
LYMPHEDEMA-DISTICHIASIS AND FOXC2 GENE MUTATIONS
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Vol 31, No 4 (1998) - Articles
PHENOTYPIC AND GENOTYPIC HETEROGENEITY IN FAMILIAL MILROY LYMPHEDEMA
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Vol 47, No 1 (2014) - Articles
A NOVEL FLT4 GENE MUTATION IDENTIFIED IN A PATIENT WITH MILROY DISEASE
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Vol 47, No 4 (2014) - Articles
NEXT GENERATION SEQUENCING IS HERE NOW
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Vol 51, No 2 (2018) - Articles
FROM CHILDHOOD ONSET LYMPHEDEMA TO FATAL FETAL HYDROPS: POSSIBLE MODIFYING GENES FOR A FOXC2 MUTATION
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