Severe Factor X Deficiency in a pair of siblings.: Clinical presentation, phenotypic and genotypic features , prenatal diagnosis, and optimized treatment.

Troels Herlin; Benny Sørensen; Niels Clausen; K Chu; Jørgen Ingerslev; K High

Severe Factor X Deficiency in a pair of siblings. Clinical presentation, phenotypic and genotypic features , prenatal diagnosis, and optimized treatment.

Troels Herlin, Benny Sørensen, Niels Clausen, K Chu, Jørgen Ingerslev, K High

Research output: Contribution to conference › Poster › Research

Original language	English
Publication date	2006
Publication status	Published - 2006
Event	World Federation of Hemophilia - Vancouver, Canada Duration: 20 May 2006 → 25 May 2006

Conference

Conference	World Federation of Hemophilia
Country/Territory	Canada
City	Vancouver
Period	20/05/2006 → 25/05/2006

Cite this

@conference{0d2649205eeb11dbbee902004c4f4f50,

title = "Severe Factor X Deficiency in a pair of siblings.: Clinical presentation, phenotypic and genotypic features , prenatal diagnosis, and optimized treatment.",

author = "Troels Herlin and Benny S{\o}rensen and Niels Clausen and K Chu and J{\o}rgen Ingerslev and K High",

year = "2006",

language = "English",

note = "World Federation of Hemophilia ; Conference date: 20-05-2006 Through 25-05-2006",

}