Prenatal DNA diagnosis of a single-gene disorder from maternal plasma

Lancet

Volumn 356, Issue 9236, 2000, Pages 1170-

  Saito, Hiroshi ^a   Sekizawa, Akihiko ^a   Morimoto, Taro ^a   Suzuki, Makoto ^a   Yanaihara, Takumi ^a  

^a SHOWA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACHONDROPLASIA; ADULT; ARTICLE; CASE REPORT; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; FEMALE; HUMAN; HUMAN TISSUE; MATERNAL PLASMA; NON INVASIVE MEASUREMENT; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

EID: 0034734711     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)02767-7     Document Type: Article

References (4)

1. A Watanabe A Sekizawa A Taguchi Prenatal diagnosis of ornitine transcarbamylase deficiency by using a single nucleated erythrocyte from maternal blood Hum Genet 102 1998 611 615
2. YMD Lo N Corbetta PF Chamberlain V Rai IL Sargent CWG Redman Presence of fetal DNA in maternal plasma and serum Lancet 350 1997 485 487
3. YMD Lo NM Hjelm C Fidler Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma N Engl J Med 339 1998 1734 1738
4. R Shiang LM Thompson YZ Zhu Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia Cell 78 1994 335 342