Počet záznamov: 1
hemoglobinopatie
SYS d006453 LBL 00000nx--j2200000---45-- 005 20240119201015.9 100 $a 19990101asloy0103----ba0 152 $b mesh 250 $a hemoglobinopatie $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 68 $8 eng 330 1-
$a A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. $8 eng 450 $a choroby hemoglobínu $5 e $8 slo 550 $3 sllk_un_auth*d006455 $Y Hemoglobins, Abnormal $5 F $a hemoglobíny abnormálne 550 $3 sllk_un_auth*d006455 $Y Hemoglobins, Abnormal $5 B $a hemoglobíny abnormálne 686 $a C15.378.420 686 $a C16.320.365 750 $a Hemoglobinopathies $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20070706 801 -2
$a SK $b BA006 $c 20150814 820 $a do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available $8 eng 980 $x M
Počet záznamov: 1