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A novel X-linked mental retardation syndrome with short stature maps to Xq24

Autor: Vitale, E (Vitale, E), Specchia, C (Specchia, C), Devoto, M (Devoto, M), Angius, A (Angius, A), Rong, S (Rong, S), Subramanian, K (Subramanian, K), Rocchi, M (Rocchi, M), Schwalb, M (Schwalb, M), Demelas, L (Demelas, L), Paglietti, D (Paglietti, D), Manca, S (Manca, S), Mastropaolo, C (Mastropaolo, C), Serra, G (Serra, G)

Publikováno v: American journal of human genetics 67 (2000): 332–332.
info:cnr-pdr/source/autori:Vitale, E (Vitale, E); Specchia, C (Specchia, C); Devoto, M (Devoto, M); Angius, A (Angius, A); Rong, S (Rong, S); Subramanian, K (Subramanian, K); Rocchi, M (Rocchi, M); Schwalb, M (Schwalb, M); Demelas, L (Demelas, L); Paglietti, D (Paglietti, D); Manca, S (Manca, S); Mastropaolo, C (Mastropaolo, C); Serra, G (Serra, G)/titolo:A novel X-linked mental retardation syndrome with short stature maps to Xq24./doi:/rivista:American journal of human genetics/anno:2000/pagina_da:332/pagina_a:332/intervallo_pagine:332–332/volume:67

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::df3eeb8dd33915bbdd791daefc917e16
https://publications.cnr.it/doc/265269

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Linkage analysis conditional on HLA status supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12

Autor: Vitale, E, Devoto, M, Sun, R, Specchia, Claudia, Subramaian, K, Rocchi, M, Schwalb, M, Nathanson, D, ROHOWSKY KOCHAN, C, Cook, S.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3662::207508b8a3b1c325edc968be7722c967
http://hdl.handle.net/11379/22990

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Genome Mapping of Multiple Sclerosis in alarge American pedigree

Autor: Vitale E., Devoto M., Sun R., Rohowsky-Kochan C., NathansonD., Schwalb M., Cook S.

Publikováno v: American journal of human genetics (1999).
info:cnr-pdr/source/autori:Vitale E., Devoto M., Sun R., Rohowsky-Kochan C., NathansonD., Schwalb M., Cook S./titolo:Genome Mapping of Multiple Sclerosis in alarge American pedigree./doi:/rivista:American journal of human genetics/anno:1999/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::9ddabdfe37697114bb5a1f91a5494ae8
http://www.cnr.it/prodotto/i/19361

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Linkage studies of non syndromic recessive deafness in a Turkishkindred which segregates DFNB9

Autor: Leal S.M., Apaydin F., Barnwell C., Iber M., Kandogan T., Cura O., Braendle O., Zenner H.P., Schwalb M., Vitale E.

Publikováno v: European journal of human genetics (1998).
info:cnr-pdr/source/autori:Leal S.M., Apaydin F., Barnwell C., Iber M., Kandogan T.,Cura O., Braendle O., Zenner H.P., Schwalb M., Vitale E./titolo:Linkage studies of non syndromic recessive deafness in a Turkishkindred which segregates DFNB9./doi:/rivista:European journal of human genetics/anno:1998/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::b07dae5f800ae14a56fec5856c7507e3
https://publications.cnr.it/doc/19368

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