Login
|
New Account
AAAAAA
ITA
ENG
Results:
1-2
|
Results: 2
Smith-Lemli-Opitz (RHS) syndrome: Holoprosencephaly and homozygous IVS8-1G-> C genotype
Authors:
Nowaczyk, MJM Farrell, SA Sirkin, WL Velsher, L Krakowiak, PA Waye, JS Porter, FD
Citation:
Mjm. Nowaczyk et al., Smith-Lemli-Opitz (RHS) syndrome: Holoprosencephaly and homozygous IVS8-1G-> C genotype, AM J MED G, 103(1), 2001, pp. 75-80
Lethal neonatal Menkes' disease with severe vasculopathy and fractures
Authors:
Jankov, RP Boerkoel, CF Hellmann, J Sirkin, WL Tumer, Z Horn, N Feigenbaum, A
Citation:
Rp. Jankov et al., Lethal neonatal Menkes' disease with severe vasculopathy and fractures, ACT PAEDIAT, 87(12), 1998, pp. 1297-1300
Risultati:
1-2
|