Sfoglia per Autore
A 46,XY infant with uterus, dysgenetic gonads and multiple anomalies
1974-01-01 Silengo M; Kaufman RL; Kissane J.
Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome.
1976-01-01 Silengo MC; Andria G
Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome
1977-01-01 Silengo MC; Franceschini P; Cerutti A; Fabris C
Pseudo-pseudohermaphroditism and multiple neurofibromatosis
1978-01-01 Franceschini P; Silengo M; Davi GF
Monosomia parziale 7q
1978-01-01 Franceschini P; Silengo M; Davi G
Appendice : analisi del cariotipo umano
1978-01-01 Franceschini P; Cirillo Silengo M; Davi G
Recessive spondylocostal dysostosis: two new cases
1978-01-01 Silengo MC; Cavallaro S; Franceschini P
Trisomy-8 mosaicism: report of a case
1978-01-01 Silengo MC; Davi G; Crua G; Franceschini P
The 49XXXXX syndrome. Report of a case with 48XXXX/49XXXXX mosaicism
1979-01-01 Cirillo Silengo M; Davi GF; Franceschini P
Radiological features in trisomy 8
1979-01-01 Silengo MC; Davi GF; Franceschini P
The syndrome of trisomy 22; clinico-immunological findings
1979-01-01 Davi GF; Silengo M; Bertone M; Franceschini P
Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter)
1979-01-01 Franceschini P; Silengo MC; Davi GF; Santoro MA; Prandi G; Fabris C.
Clinical and genetic aspects of Conradi-Hünermann disease. A report of three familial cases and review of the literature.
1980-01-01 Silengo MC; Luzzatti L; Silverman FN.
Rhizomelic type of chondrodysplasia punctata in 2 sisters. Evidence for hereditary transmission of a recessive autosomic type
1981-01-01 Fabris C; Licata D; Martano C; Silengo M; Franceschini P
Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation
1981-01-01 Silengo MC; Luzzatti L; Centerwall WR; Costello JM; Parslow M
Interstitial deletion of the short arm of chromosome 7 without craniosynostosis
1981-01-01 Bianchi DW; Cirillo Silengo M; Luzzatti L; Greenstein RM
Trisomy 22: a clinical diagnosis
1981-01-01 Cirillo Silengo M; Davi G; Bianco R; Costa M; De Marco A; Franceschini P
Cryptorchism: genetics and epigenetics
1982-01-01 Franceschini P; Davi GF; Bianco R; Silengo M
Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndrome
1982-01-01 Silengo MC; Davi GF; Bianco R; Costa M; DeMarco A; Verona R; Franceschini P
Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies
1982-01-01 Silengo MC; Davi GF; Franceschini P
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