IRIS

Sfoglia per Autore  GURRIERI, FIORELLA

Opzioni
Mostrati risultati da 1 a 20 di 125
Titolo Data di pubblicazione Autore(i) File
Structural and functional analysis of a growth-regulated gene, the human calcyclin. 1-gen-1987 Ferrari, S; Calabretta, B; Deriel, Jk; Battini, R; Ghezzo, F; Lauret, E; Griffin, C; Emanuel, Bs; Gurrieri, F; Baserga, R.
X-linked Mental retardation: update 1991 1-gen-1991 Neri, G; Gurrieri, F
A GIRL WITH THE LUJAN-FRYNS SYNDROME 1-gen-1991 Gurrieri, F; Neri, G
X-LINKED MENTAL-RETARDATION WITH MARFANOID HABITUS - 1ST REPORT OF 4 ITALIAN PATIENTS 1-gen-1991 Lalatta, F; Livini, E; Selicorni, A; Briscioli, V; Vita, A; Lugo, F; Zollino, M; Gurrieri, F; Neri, G
XLMR GENES - UPDATE 1990 1-gen-1991 Neri, G; Gurrieri, F; Gal, A; Lubs, Ha
AN ADDITIONAL PATIENT WITH THE 3C SYNDROME 1-gen-1992 Gurrieri, F; Neri, G
POSSIBLE NEW TYPE OF ORAL-FACIAL-DIGITAL SYNDROME WITH RETINAL ABNORMALITIES - OFDS TYPE-(VIII) 1-gen-1992 Gurrieri, F; Sammito, V; Ricci, B; Iossa, M; Bellussi, A; Neri, G
NEW AUTOSOMAL RECESSIVE SYNDROME OF MENTAL-RETARDATION, EPILEPSY, SHORT STATURE, AND SKELETAL DYSPLASIA 1-gen-1992 Gurrieri, F; Sammito, V; Bellussi, A; Neri, G
FURTHER DELINEATION OF THE SIMPSON-GOLABI-BEHMEL (SGB) SYNDROME 1-gen-1992 Gurrieri, F; Cappa, M; Neri, G
DILATED CARDIOMYOPATHY IN THE SGB SYNDROME - REPLY 1-gen-1993 Neri, G; Gurrieri, F
PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY CRITICAL REGION ON CHROMOSOME-7Q36 RID A-1081-2010 1-gen-1993 Gurrieri, F; Trask, Bj; Vandenengh, G; Krauss, Cm; Schinzel, A; Pettenati, Mj; Schindler, D; Dietzband, J; Vergnaud, G; Scherer, Sw; Tsui, Lc; Muenke, M
INHERITANCE OF THE ORAL-FACIAL-DIGITAL SYNDROME (OFDS) TYPE-VIII - REPLY 1-gen-1993 Gurrieri, F; Neri, G
Holoprosencephaly: molecular approaches toward understanding midline development of the forebrain in humans 1-gen-1994 Muenke, M; Gurrieri, F
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. 1-gen-1994 Muenke, M; Gurrieri, F; Bay, C; Yi, Dh; Collins, Al; Johnson, Vp; Hennekam, Rc; Schaefer, Gb; Weik, L; Lubinsky, Ms; Et, Al.
EXCLUSION OF LINKAGE BETWEEN AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT AND MARKERS FROM CHROMOSOME 7Q - FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY 1-gen-1994 Gurrieri, F; Genuardi, M; Chiurazzi, P; Gillessenkaesbach, G; Neri, G
SIMPSON-GOLABI-BEHMEL GENE IS CLOSELY LINKED TO HPRT IN XQ26 IN 2 EUROPEAN FAMILIES 1-gen-1994 Xu, S; Orth, U; Gurrieri, F; Cremer, M; Behmel, A; Genuardi, M; Neri, G; Gal, A
FINE MAPPING OF THE AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT LOCUS ON CHROMOSOME-7, BAND Q21.3-Q22.1 RID A-1081-2010 1-gen-1994 Scherer, Sw; Poorkaj, P; Allen, T; Kim, J; Geshuri, D; Nunes, M; Soder, S; Stephens, K; Pagon, Ra; Patton, Ma; Berg, Ma; Donlon, T; Rivera, H; Pfeiffer, Ra; Naritomi, K; Hughes, H; Genuardi, M; Gurrieri, F; Neri, G; Lovrein, E; Magenis, E; Tsui, Lc; Evans, Jp
GENES FOR SPLIT HAND/SPLIT FOOT AND LATERALITY DEFECTS ON 7Q22.1 AND XQ24-Q27.1 1-gen-1994 Genuardi, M; Gurrieri, F; Neri, G
GENE FOR SIMPSON-GOLABI-BEHMEL SYNDROME IS LINKED TO HPRT IN XQ26 IN 2 EUROPEAN FAMILIES 1-gen-1994 Orth, U; Gurrieri, F; Behmel, A; Genuardi, M; Cremer, M; Gal, A; Neri, G
ORAL-FACIAL-SKELETAL SYNDROMES 1-gen-1995 Neri, G; Gurrieri, F; Genuardi, M
Mostrati risultati da 1 a 20 di 125
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile