|1.||Kusre, Giriraj: 1 article (05/2015)|
|2.||Goswami, Dibyajyoti: 1 article (05/2015)|
|3.||Tantau, J: 1 article (09/2013)|
|4.||Kaplan, J: 1 article (09/2013)|
|5.||Chassaing, N: 1 article (09/2013)|
|6.||van Tintelen, J P: 1 article (09/2013)|
|7.||Corsten-Janssen, N: 1 article (09/2013)|
|8.||Patat, O: 1 article (09/2013)|
|9.||Dijkhuizen, T: 1 article (09/2013)|
|10.||van Ravenswaaij-Arts, C M A: 1 article (09/2013)|
05/01/2015 - "To the best of our knowledge this is the first case of agnathia, holoprosencephaly and situs inversus complex to be reported in an indexed literature from India. "
05/01/2015 - "Hereby, we are presenting a case of agnathia, holoprosencephaly and situs inversus born at 32 wk of gestation by an alcoholic mother. "
05/01/2015 - "Agnathia, holoprosencephaly and situs inversus complex is an extremely rare form of congenital malformation. "
05/01/2015 - "Agnathia Holoprosencephaly and Situs Inversus in A Neonate Born to an Alcoholic Mother."
09/01/2002 - "The sixth clinical report of a rare association: agnathia-holoprosencephaly-situs inversus."
09/01/2013 - "Otocephaly-dysgnathia complex is characterized by mandibular hypo- or aplasia, ear abnormalities, microstomia, and microglossia. "
06/01/2012 - "Otocephaly or dysgnathia complex is characterised by mandibular hypoplasia/agenesis, ear anomalies, microstomia, and microglossia; the molecular basis of this developmental defect is largely unknown in humans. "
02/01/2007 - "The dysgnathia complex (agnathia-otocephaly) (AO) is a lethal malformation that consists of congenital absence of the lower jaw with union or close approximation of the lower ears on the front of the neck, microstomia, and hypoglossia. "
07/01/1991 - "The rare syndrome of the agnathia with microstomia, aglossia, synotia (the external ears approaching one another in the midline) and brain malformation (agnathia-holoprosencephaly) was reported by Pauli et al. (1983) as a developmental field defect. "
01/01/2013 - "Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosology."
01/01/1992 - "Analysing literature cases and the case presented here we can suggest that: 1) not only alobar holoprosencephaly but also more severe forebrain anomalies can be a brain equivalent of cyclopia; 2) aprosencephaly can be viewed as the earliest known variant of prosencephalic series; and 3) "agnathia-holoprosencephaly" association is etiologically heterogeneous."