Co-existence of Bernard Soulier syndrome and factor XI deficiency in a family: A unified pathology?

Platelets

Volumn 16, Issue 2, 2005, Pages 85-89

  Ghosh, K ^a   Nair, S ^a   Shetty, S ^a   Rajapurkar, M ^a   Mohanty, D ^a  

^a NATIONAL INSTITUTE OF IMMUNOHAEMATOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 11; TRANSCRIPTION FACTOR;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; BERNARD SOULIER DISEASE; BLEEDING TENDENCY; BLOOD CLOTTING FACTOR 11 DEFICIENCY; CASE REPORT; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CLINICAL FEATURE; ECCHYMOSIS; FAMILY HISTORY; HETEROZYGOTE; HUMAN; HUMAN TISSUE; INDIA; KARYOTYPE; MALE; PEDIGREE; PETECHIA; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROCESSING; SCHOOL CHILD; SYMPTOM;

BERNARD-SOULIER SYNDROME; CHILD; CHROMOSOMES; FACTOR XI DEFICIENCY; HUMANS; KARYOTYPING; MALE; PEDIGREE; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC;

RAPHIA FRATER;

EID: 17144363869     PISSN: 09537104     EISSN: None     Source Type: Journal    
DOI: 10.1080/09537100400010345     Document Type: Article

References (11)

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