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Results:
1-11
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Results: 11
Authors:
Shotelersuk, V
Ittiwut, C
Shotelersuk, K
Triratanachat, S
Poovorawan, Y
Mutirangura, A
Citation: V. Shotelersuk et al., Fibroblast growth factor receptor 3 S249C mutation in virus associated squamous cell carcinomas, ONCOL REP, 8(6), 2001, pp. 1301-1304
Authors:
Shotelersuk, V
Punyavoravud, V
Phudhichareonrat, S
Kukulprasong, A
Citation: V. Shotelersuk et al., An Asian girl with a 'milder' form of the Hydrolethalus syndrome, CLIN DYSMOR, 10(1), 2001, pp. 51-55
Authors:
Shotelersuk, V
Goyal, M
Rauchenstein, JN
Konez, O
Citation: V. Shotelersuk et al., Subdural empyema secondary to odontogenic masticator space abscess: Detection by indium-111-labeled white cell scan, CLIN IMAG, 25(1), 2001, pp. 18-22
Authors:
Touchman, JW
Anikster, Y
Dietrich, NL
Maduro, VVB
McDowell, G
Shotelersuk, V
Bouffard, GG
Beckstrom-Sternberg, SM
Gahl, WA
Green, ED
Citation: Jw. Touchman et al., The genomic region encompassing the nephropathic cystinosis gene (CTNS): Complete sequencing of a 200-kb segment and discovery of a novel gene withinthe common cystinosis-causing deletion, GENOME RES, 10(2), 2000, pp. 165-173
Authors:
Anikster, Y
Lucero, C
Guo, JR
Huizing, M
Shotelersuk, V
Bernardini, I
McDowell, G
Iwata, F
Kaiser-Kupfer, MI
Jaffe, R
Thoene, J
Schneider, JA
Gahl, WA
Citation: Y. Anikster et al., Ocular nonnephropathic cystinosis: Clinical, biochemical, and molecular correlations, PEDIAT RES, 47(1), 2000, pp. 17-23
Authors:
Brantly, M
Avila, NA
Shotelersuk, V
Lucero, C
Huizing, M
Gahl, WA
Citation: M. Brantly et al., Pulmonary function and high-resolution CT findings in patients with an inherited form of pulmonary fibrosis, Hermansky-Pudlak syndrome, due to mutations in HPS-1, CHEST, 117(1), 2000, pp. 129-136
Authors:
Shotelersuk, V
Dell'Angelica, EC
Hartnell, L
Bonifacino, JS
Gahl, WA
Citation: V. Shotelersuk et al., A new variant of Hermansky-Pudlak syndrome due to mutations in a gene responsible for vesicle formation, AM J MED, 108(5), 2000, pp. 423-427
Authors:
Dell'Angelica, EC
Shotelersuk, V
Aguilar, RC
Gahl, WA
Bonifacino, JS
Citation: Ec. Dell'Angelica et al., Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome dueto mutations in the beta 3A subunit of the AP-3 adaptor, MOL CELL, 3(1), 1999, pp. 11-21
Authors:
Anikster, Y
Lucero, C
Touchman, JW
Huizing, M
McDowell, G
Shotelersuk, V
Green, ED
Gahl, WA
Citation: Y. Anikster et al., Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS), MOL GEN MET, 66(2), 1999, pp. 111-116
Authors:
Anikster, Y
Shotelersuk, V
Gahl, WA
Citation: Y. Anikster et al., CTNS mutations in patients with cystinosis, HUM MUTAT, 14(6), 1999, pp. 454-458
Authors:
Shotelersuk, V
Tifft, CJ
Vacha, S
Peters, KF
Biesecker, LG
Citation: V. Shotelersuk et al., Discordance of oral-facial-digital syndrome type 1 in monozygotic twin girls, AM J MED G, 86(3), 1999, pp. 269-273
Risultati:
1-11
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