Results
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23.
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A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere. [electronic resource] by
- Gianfrancesco, F
- Esposito, T
- Montanini, L
- Ciccodicola, A
- Mumm, S
- Mazzarella, R
- Rao, E
- Giglio, S
- Rappold, G
- Forabosco, A
Producer: 19980416
In:
Human molecular genetics vol. 7
Availability: No items available.
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24.
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A novel germline mutation in peroxisome proliferator-activated receptor gamma gene associated with large intestine polyp formation and dyslipidemia. [electronic resource] by
- Capaccio, D
- Ciccodicola, A
- Sabatino, L
- Casamassimi, A
- Pancione, M
- Fucci, A
- Febbraro, A
- Merlino, A
- Graziano, G
- Colantuoni, V
Producer: 20100622
In:
Biochimica et biophysica acta vol. 1802
Availability: No items available.
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25.
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26.
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Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes. [electronic resource] by
- Ciccodicola, A
- Cinti, C
- Esposito, T
- Campanile, C
- Casamassimi, A
- Miano, M G
- Maraldi, N M
- Vitale, M
- Johnson, D
- Molini, B
Producer: 19941228
In:
Mammalian genome : official journal of the International Mammalian Genome Society vol. 5
Availability: No items available.
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27.
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YAC contig organization and CpG island analysis in Xq28. [electronic resource] by
- Palmieri, G
- Romano, G
- Ciccodicola, A
- Casamassimi, A
- Campanile, C
- Esposito, T
- Cappa, V
- Lania, A
- Johnson, S
- Reinbold, R
Producer: 19950421
In:
Genomics vol. 24
Availability: No items available.
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28.
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SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function. [electronic resource] by
- Nigro, V
- Bruni, P
- Ciccodicola, A
- Politano, L
- Nigro, G
- Piluso, G
- Cappa, V
- Covone, A E
- Romeo, G
- D'Urso, M
Producer: 19960418
In:
Human molecular genetics vol. 4
Availability: No items available.
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29.
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Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosa. [electronic resource] by
- Simonelli, F
- Rinaldi, M
- Nesti, A
- Testa, F
- Rinaldi, E
- Ciccodicola, A
- Flagiello, L
- Miano, M G
- Ventruto, V
- D'Urso, M
Producer: 19981106
In:
The British journal of ophthalmology vol. 82
Availability: No items available.
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30.
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Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease. [electronic resource] by
- Bione, S
- Small, K
- Aksmanovic, V M
- D'Urso, M
- Ciccodicola, A
- Merlini, L
- Morandi, L
- Kress, W
- Yates, J R
- Warren, S T
Producer: 19960418
In:
Human molecular genetics vol. 4
Availability: No items available.
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31.
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An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence. [electronic resource] by
- D'Urso, M
- Luzzatto, L
- Perroni, L
- Ciccodicola, A
- Gentile, G
- Peluso, I
- Persico, M G
- Pizzella, T
- Toniolo, D
- Vulliamy, T J
Producer: 19880526
In:
American journal of human genetics vol. 42
Availability: No items available.
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32.
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ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations. [electronic resource] by
- Gianfrancesco, F
- Esposito, T
- Penco, S
- Maglione, V
- Liquori, C L
- Patrosso, M C
- Zuffardi, O
- Ciccodicola, A
- Marchuk, D A
- Squitieri, F
Producer: 20081203
In:
Neuroscience vol. 155
Availability: No items available.
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33.
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Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. [electronic resource] by
- Vervoort, R
- Lennon, A
- Bird, A C
- Tulloch, B
- Axton, R
- Miano, M G
- Meindl, A
- Meitinger, T
- Ciccodicola, A
- Wright, A F
Producer: 20000828
In:
Nature genetics vol. 25
Availability: No items available.
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34.
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Human dbl proto-oncogene in 85 kb of xq26, and determination of the transcription initiation site. [electronic resource] by
- Palmieri, G
- de Franciscis, V
- Casamassimi, A
- Romano, G
- Torino, A
- Pingitore, P
- Califano, D
- Santelli, G
- Eva, A
- Vecchio, G
- D'Urso, M
- Ciccodicola, A
Producer: 20000921
In:
Gene vol. 253
Availability: No items available.
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35.
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Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes. [electronic resource] by
- Aradhya, S
- Bardaro, T
- Galgóczy, P
- Yamagata, T
- Esposito, T
- Patlan, H
- Ciccodicola, A
- Munnich, A
- Kenwrick, S
- Platzer, M
- D'Urso, M
- Nelson, D L
Producer: 20020221
In:
Human molecular genetics vol. 10
Availability: No items available.
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36.
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Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families. [electronic resource] by
- Simonelli, F
- Cennamo, G
- Ziviello, C
- Testa, F
- de Crecchio, G
- Nesti, A
- Manitto, M P
- Ciccodicola, A
- Banfi, S
- Brancato, R
- Rinaldi, E
Producer: 20031016
In:
The British journal of ophthalmology vol. 87
Availability: No items available.
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37.
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Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci. [electronic resource] by
- Chen, E Y
- Zollo, M
- Mazzarella, R
- Ciccodicola, A
- Chen, C N
- Zuo, L
- Heiner, C
- Burough, F
- Repetto, M
- Schlessinger, D
- D'Urso, M
Producer: 19970604
In:
Human molecular genetics vol. 5
Availability: No items available.
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38.
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Human and mouse SYBL1 gene structure and expression. [electronic resource] by
- Matarazzo, M R
- Cuccurese, M
- Strazzullo, M
- Vacca, M
- Curci, A
- Miano, M G
- Cocchia, M
- Mercadante, G
- Torino, A
- D'Urso, M
- Ciccodicola, A
- D'Esposito, M
Producer: 20000111
In:
Gene vol. 240
Availability: No items available.
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39.
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Expressed STSs and transcription of human Xq28. [electronic resource] by
- Esposito, T
- Ciccodicola, A
- Flagiello, L
- Matarazzo, M R
- Migliaccio, C
- Cifarelli, R A
- Visone, R
- Campanile, C
- Mazzarella, R
- Schlessinger, D
- D'Urso, M
- D'Esposito, M
Producer: 19970520
In:
Gene vol. 187
Availability: No items available.
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40.
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Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families. [electronic resource] by
- Ziviello, C
- Simonelli, F
- Testa, F
- Anastasi, M
- Marzoli, S B
- Falsini, B
- Ghiglione, D
- Macaluso, C
- Manitto, M P
- Garrè, C
- Ciccodicola, A
- Rinaldi, E
- Banfi, S
Producer: 20060518
In:
Journal of medical genetics vol. 42
Availability: No items available.
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