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



Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
Times Cited: 221




List of shared articles



Times cited

Syndromes associated with holoprosencephaly.
Paul Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
23

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

Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, Göran Annerén, Marian Bakker, Fabrizio Bianchi, Carol Bower, Mark A Canfield, Eduardo E Castilla, Guido Cocchi,[...]. Birth Defects Res A Clin Mol Teratol 2008
64

Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
36

Nationwide epidemiological survey of holoprosencephaly in Japan.
Yuichi Abe, Ryuichiro Araki, Hisanori Sobajima, Masanori Tamura, Tetsuya Kunikata, Akira Ohtake, Hideo Yamanouchi. Pediatr Int 2020
0