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Statements

Subject Item
n2:RIV%2F00064165%3A_____%2F01%3A00000372%21RIV%2F2002%2FGA0%2FL38002%2FN
rdf:type
skos:Concept n17:Vysledek
dcterms:description
Rett syndrome Rett syndrome
dcterms:title
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
skos:prefLabel
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
skos:notation
RIV/00064165:_____/01:00000372!RIV/2002/GA0/L38002/N
n3:strany
281;281
n3:aktivita
n14:P
n3:aktivity
P(GA201/00/P068), P(GA302/99/0648), P(GP301/01/P068)
n3:cisloPeriodika
Suppl. 1
n3:dodaniDat
n15:2002
n3:domaciTvurceVysledku
n7:5651077 n7:4688678 n7:6270875
n3:druhVysledku
n10:J
n3:duvernostUdaju
n16:S
n3:entitaPredkladatele
n13:predkladatel
n3:idSjednocenehoVysledku
687565
n3:idVysledku
RIV/00064165:_____/01:00000372
n3:jazykVysledku
n9:eng
n3:klicovaSlova
Molecular;diagnosis;syndrome;Detection;prevalent;mutation;MeCP2;Czech;Slovak;patients
n3:klicoveSlovo
n8:Detection n8:prevalent n8:MeCP2 n8:patients n8:diagnosis n8:Czech n8:mutation n8:Molecular n8:Slovak n8:syndrome
n3:kodStatuVydavatele
GB - Spojené království Velké Británie a Severního Irska
n3:kontrolniKodProRIV
[D72B5A52A1F7]
n3:nazevZdroje
European Journal of Human Genetics
n3:obor
n12:FL
n3:pocetDomacichTvurcuVysledku
3
n3:pocetTvurcuVysledku
5
n3:pocetUcastnikuAkce
0
n3:pocetZahranicnichUcastnikuAkce
0
n3:projekt
n4:GP301%2F01%2FP068 n4:GA302%2F99%2F0648 n4:GA201%2F00%2FP068
n3:rokUplatneniVysledku
n15:2001
n3:svazekPeriodika
9
n3:tvurceVysledku
Martásek, Pavel Zeman, Jiří Rosipal, Robert
s:issn
1018-4813
s:numberOfPages
1