Author:
Dubucs C.,Chassaing N.,Sergi C.,Aubert-Mucca M.,Attié-Bitach T.,Lacombe D.,Thauvin-Robinet C.,Arpin S.,Perez M. J.,Cabrol C.,Chen C. P.,Aziza J.,Colin E.,Martinovic J.,Calvas P.,Plaisancié Julie
Publisher
Springer Science and Business Media LLC
Reference63 articles.
1. Pauli RM, Pettersen JC, Arya S, Gilbert EF (1983) Familial agnathia-holoprosencephaly. Am J Med Genet 14(4):677–698. https://doi.org/10.1002/ajmg.1320140411
2. Gaba AR, Anderson GJ, VanDyke DL, Chason JL (1982) Alobar holoprosencephaly and otocephaly in a female infant with a normal karyotype and placental villitis. J Med Genet 19(1):78
3. Carles D, Serville F, Mainguene M, Dubecq JP (1987) Cyclopia-otocephaly association: a new case of the most severe variant of agnathia-holoprosencephaly complex. J Craniofac Genet Dev Biol 7(2):107–113
4. Hersh JH, McChane RH, Rosenberg EM, Powers WH Jr, Corrigan C, Pancratz L (1989) Otocephaly-midline malformation association. Am J Med Genet 34(2):246–249. https://doi.org/10.1002/ajmg.1320340223
5. Blaas HG, Eriksson AG, Salvesen KA, Isaksen CV, Christensen B, Mollerlokken G, Eik-Nes SH (2002) Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases. Ultrasound Obstet Gynecol 19(1):24–38. https://doi.org/10.1046/j.0960-7692.2001.00154.x
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