Homozygous protein C deficiency detectable by prenatal diagnosis;Fosterdiagnostik kan avslöja homozygot protein C-brist

Lakartidningen

Volumn , Issue 36, 1998, Pages 3772-3777

  Jerkeman, Anna ^a   Henriksson, Per ^b   Jonsson, Nils Olof ^c   Berntorp, Erik ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b Overlakare Barn Och U   (Sweden)

^c Barnmedicinska Kliniken   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN C;

ADULT; ANAPHYLACTOID PURPURA; ARTICLE; BLOOD CLOTTING DISORDER; CASE REPORT; FEMALE; GENETICS; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMAN; INFANT; MALE; NEWBORN; POINT MUTATION; PREGNANCY; PRENATAL DIAGNOSIS; PROTEIN C DEFICIENCY;

ADULT; BLOOD COAGULATION DISORDERS; FEMALE; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; MALE; POINT MUTATION; PREGNANCY; PRENATAL DIAGNOSIS; PROTEIN C; PROTEIN C DEFICIENCY; PURPURA, SCHOENLEIN-HENOCH;

EID: 0032475251     PISSN: 00237205     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

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