Prenatal diagnosis of Glanzmann thrombasthenia

National Medical Journal of India

Volumn 16, Issue 4, 2003, Pages 207-208

  Srivastava, Alok ^a   Usher, Saly ^b   Nelson, Everette J R ^a   Jayandharan, G ^a   Shaji, Ramachandran V ^a   Chandy, Mammen ^a   Seligsohn, Uri ^c   Peretz, Hava ^b  

^a CHRISTIAN MEDICAL COLLEGE   (India)

^b TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

^c SHEBA MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; BRCA1 PROTEIN; CYTOSINE; FIBRINOGEN RECEPTOR; SMAD PROTEIN; TAQ POLYMERASE; TYROSINE;

ADULT; ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BLEEDING; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 17Q; CHROMOSOME MARKER; DINUCLEOTIDE REPEAT; EXON; FAMILY STUDY; FEMALE; FETUS; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC POLYMORPHISM; GLANZMANN DISEASE; HAPLOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; INDIA; INHERITANCE; INTRON; MALE; MENORRHAGIA; MORBIDITY; PRENATAL DIAGNOSIS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; THROMBOCYTE FUNCTION;

ADULT; CHILD; FEMALE; GENETIC TECHNIQUES; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INDIA; MALE; PRENATAL DIAGNOSIS; THROMBASTHENIA;

EID: 0142248326     PISSN: 0970258X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

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2. French DL, Coller BS, Usher S, Berkowitz R, Eng C, Seligsohn U, et al. Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17. Br J Haematol 1998;102:582-7.
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