|1.||Townsend, Jeanette J: 1 article (11/2005)|
|2.||Bizzarri, C: 1 article (11/2005)|
|3.||Opitz, John M: 1 article (11/2005)|
|4.||Chessa, L: 1 article (11/2005)|
|5.||Vignati, E: 1 article (11/2005)|
|6.||Miller, Mark E: 1 article (11/2005)|
|7.||Byrne, Janice L: 1 article (11/2005)|
|8.||Renzetti, G: 1 article (11/2005)|
|9.||Cappa, M: 1 article (11/2005)|
|10.||Szakacs, Juliana: 1 article (11/2005)|
09/15/1993 - "We report on a stillborn male infant with a mosaic ring 13 karyotype (45,XY,-13/46,XY,-13,+r(13)) with apparent aprosencephaly and clinical findings similar to those reported previously in the XK-aprosencephaly syndrome. "
03/01/1988 - "The coexistence of anencephaly and aprosencephaly within a sibship suggests that XK aprosencephaly syndrome may be an autosomal recessive disorder."
03/01/1988 - "XK aprosencephaly and anencephaly in sibs."
03/01/1982 - "A review and case report of aprosencephaly and the XK aprosencephaly syndrome."
08/01/2004 - "XK aprosencephaly, also called Garcia-Lurie syndrome (GLS), is a usually sporadic disorder with radial limb defects and aprosencephaly/atelencephaly. "
|3.||Disorders of Sex Development (Intersexuality)
10/31/1997 - "We report on a patient with a multiple congenital abnormalities/mental retardation (MCA/MR) syndrome including facial abnormalities, agenesis of the corpus callosum, heart defect, 1st ray anomalies of the upper limb, and ambiguous genitalia, whose phenotype overlaps a previous description of XK syndrome. "
|4.||Neural Tube Defects (Exencephaly)
|2.||Craniosynostosis radial aplasia syndrome