Počet záznamov: 1
The metabolic and molecular bases of inherited disease. Vol. 3
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$a eng 102 $a US 105 $a y z 000yy 200 1-
$a <The> metabolic and molecular bases of inherited disease. Vol. 3 $f edit. Charles R. Scriver ... [et al.] $g consulting edit. John B. Stanbury, James B. Wyngaarden, Donald S. Fredrickson 205 $a 7th ed. 210 $a New York $c McGraw-Hill $d 1995 215 $a s. 36, 3181-4605, I-93 541 1-
$a Metabolický a molekulárny základ dedičných chorôb $z slo 606 $a choroby genetické, vrodené $2 mesh $3 sllk_un_auth*d030342 606 $a choroby metabolické $2 mesh $3 sllk_un_auth*d008659 606 $a poruchy metabolizmu, vrodené $2 mesh $3 sllk_un_auth*d008661 606 $a faktory hemokoagulačné $2 mesh $3 sllk_un_auth*d001779 606 $3 sllk_un_auth*d001778 $a poruchy hemokoagulácie $2 mesh 606 $a deficit vitamínu K $2 mesh $3 sllk_un_auth*d014813 606 $a fibrinogén $x biosyntéza $2 mesh $3 sllk_un_auth*d005340 606 $a deficit faktora XIII $2 mesh $3 sllk_un_auth*d005177 606 $a hemofília A $2 mesh $3 sllk_un_auth*d006467 606 $a faktor VIII $2 mesh $3 sllk_un_auth*d005169 606 $3 sllk_un_auth*d014842 $a von Willebrandove choroby $2 mesh 606 $a antitrombíny $x deficit $2 mesh $3 sllk_un_auth*d000991 606 $a hemoglobinopatie $2 mesh $3 sllk_un_auth*d006453 606 $a deficit glukózafosfátdehydrogenázy $2 mesh $3 sllk_un_auth*d005955 606 $a glykozúria renálna $2 mesh $3 sllk_un_auth*d006030 606 $a syndrómy malabsorpčné $2 mesh $3 sllk_un_auth*d008286 606 $a cystinúria $2 mesh $3 sllk_un_auth*d003555 606 $a Hartnupova choroba $2 mesh $3 sllk_un_auth*d006250 606 $a Fanconiho syndróm $2 mesh $3 sllk_un_auth*d005198 606 $a syndróm okulocerebrorenálny $2 mesh $3 sllk_un_auth*d009800 606 $a fibróza cystická $2 mesh $3 sllk_un_auth*d003550 606 $a T-lymfocyty $x patológia $2 mesh $3 sllk_un_auth*d013601 606 $a Kartagenerov syndróm $2 mesh $3 sllk_un_auth*d007619 606 $a Marfanov syndróm $2 mesh $3 sllk_un_auth*d008382 606 $a kardiomyopatia hypertrofická $2 mesh $3 sllk_un_auth*d002312 606 $a retinitis pigmentosa $2 mesh $3 sllk_un_auth*d012174 606 $a chorioiderémia $2 mesh $3 sllk_un_auth*d015794 606 $a albinizmus $2 mesh $3 sllk_un_auth*d000417 606 $a Cockayneov syndróm $2 mesh $3 sllk_un_auth*d003057 606 $a Huntingtonova choroba $2 mesh $3 sllk_un_auth*d006816 606 $a Charcotova-Marieho-Toothova choroba $2 mesh $3 sllk_un_auth*d002607 606 $a Waardenburgov syndróm $2 mesh $3 sllk_un_auth*d014849 606 $a Schilderova difúzna cerebrálna skleróza $2 mesh $3 sllk_un_auth*d002549 606 $a neurofibromatóza 2 $2 mesh $3 sllk_un_auth*d016518 675 $a 616-008.9-056.7:575.1 $v 1. stred. $z slo 702 -1
$3 sllk_un_auth*p0005544 $a Scriver $b Charles R. $f 1930- $4 340 702 -1
$a Stanbury $b John B. $3 sllk_un_auth*p0005545 $4 340 702 -1
$a Wyngaarden $b James B. $3 sllk_un_auth*p0002167 $4 340 702 -1
$a Fredrickson $b Donald S. $3 sllk_un_auth*p0005546 $4 340 801 -0
$a SK $b BA006 $c 19981223 $g AACR2
Počet záznamov: 1