A citation-based method for searching scientific literature

M Urioste, E Valcarcel, M A Gomez, I Pinel, R Garcia de León, A Diaz de Bustamante, R Tebar, M L Martinez-Frias. Am J Med Genet 1988
Times Cited: 29



S Y Pi, R M Fineman, S D Wing, M Grunnet, G Chan. Am J Med Genet 1980
Times Cited: 26




List of shared articles



Times cited

A case of trisomy 21 with holoprosencephaly: the fifth case.
H Hamada, T Arinami, M Koresawa, T Kubo, H Hamaguchi, H Iwasaki. Jinrui Idengaku Zasshi 1991
3




Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).
L L Estabrooks, K W Rao, R P Donahue, A S Aylsworth. Am J Med Genet 1990
41



Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
G Corsello, P Buttitta, M Cammarata, A Lo Presti, E Maresi, L Zumpani, L Giuffrè. Am J Med Genet 1990
18

Down syndrome (trisomy 21) with premaxillary agenesis and semilobar holoprosencephaly.
Sriparna Basu, Ashok Kumar, B K Das. Am J Med Genet A 2009
4



Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.
S A Rasmussen, C A Moore, M J Khoury, J F Cordero. Am J Med Genet 1996
41