114 related articles for article (PubMed ID: 9571288)
1. XK aprosencephaly.
al-Gazali LI; Bakalinova D; Bakir M; Nath KN
Clin Dysmorphol; 1998 Apr; 7(2):143-7. PubMed ID: 9571288
[TBL] [Abstract][Full Text] [Related]
2. Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
Lurie IW; Nedzved MK; Lazjuk GI; Kirillova IA; Cherstvoy ED
Am J Med Genet; 1979; 3(3):301-9. PubMed ID: 114053
[TBL] [Abstract][Full Text] [Related]
3. Aprosencephaly: review of the literature and report of a case with cerebellar hypoplasia, pigmented epithelial cyst and Rathke's cleft cyst.
Kim TS; Cho S; Dickson DW
Acta Neuropathol; 1990; 79(4):424-31. PubMed ID: 2339594
[TBL] [Abstract][Full Text] [Related]
4. Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome?
McPherson E; Huff D; Dunn J; Muenke M
Birth Defects Res A Clin Mol Teratol; 2004 Aug; 70(8):537-44. PubMed ID: 15329833
[TBL] [Abstract][Full Text] [Related]
5. Atelencephalic aprosencephaly.
Harris CP; Townsend JJ; Norman MG; White VA; Viskochil DH; Pysher TJ; Klatt EC
J Child Neurol; 1994 Oct; 9(4):412-6. PubMed ID: 7822735
[TBL] [Abstract][Full Text] [Related]
6. Atelencephalic microcephaly: a case report and review of the literature.
Ippel PF; Breslau-Siderius EJ; Hack WW; van der Blij HF; Bouve S; Bijlsma JB
Eur J Pediatr; 1998 Jun; 157(6):493-7. PubMed ID: 9667407
[TBL] [Abstract][Full Text] [Related]
7. The Walker-Warburg phenotype and genotype among Irish Travellers.
Murphy AM; Sheridan M; O'Neill MB; Green A
Clin Dysmorphol; 2008 Apr; 17(2):119-120. PubMed ID: 18388782
[No Abstract] [Full Text] [Related]
8. Mosaic r(13) in an infant with aprosencephaly.
Goldsmith CL; Tawagi GF; Carpenter BF; Speevak MD; Hunter AG
Am J Med Genet; 1993 Sep; 47(4):531-3. PubMed ID: 8256818
[TBL] [Abstract][Full Text] [Related]
9. Acrofacial dysostosis with ambiguous genitalia.
Wulfsberg EA; Curtis J; Wiswell TE; Puntel RA; Levin SW
Am J Med Genet; 1990 Nov; 37(3):384-7. PubMed ID: 2260569
[TBL] [Abstract][Full Text] [Related]
10. A review and case report of aprosencephaly and the XK aprosencephaly syndrome.
Martin RA; Carey JG
Am J Med Genet; 1982 Mar; 11(3):369-71. PubMed ID: 7081301
[No Abstract] [Full Text] [Related]
11. A fetus suggesting an extension of theXK-aprosencephaly spectrum phenotype.
Kajantie E; Ammälä P; Salonen R
Clin Dysmorphol; 2002 Oct; 11(4):299-301. PubMed ID: 12402000
[TBL] [Abstract][Full Text] [Related]
12. Aprosencephaly: histopathological features of the rudimentary forebrain and retina.
Kakita A; Hayashi S; Arakawa M; Takahashi H
Acta Neuropathol; 2001 Jul; 102(1):110-6. PubMed ID: 11547946
[TBL] [Abstract][Full Text] [Related]
13. Anomalies of cerebral structures in acranial neonates.
Dambska M; Schmidt-Sidor B; Maslinska D; Laure-Kamionowska M; Kosno-Kruszewska E; Deregowski K
Clin Neuropathol; 2003; 22(6):291-5. PubMed ID: 14672507
[TBL] [Abstract][Full Text] [Related]
14. The cryptophthalmos syndrome.
Levine RS; Powers T; Rosenberg HK; Siegel CA; Bilaniuk LT
AJR Am J Roentgenol; 1984 Aug; 143(2):375-6. PubMed ID: 6430051
[No Abstract] [Full Text] [Related]
15. Triopia: craniofacial malformation with prosencephalic duplication.
Stelnicki EJ; Marsh JL; Woolsey TA; Lee BC; Noetzel MJ
Cleft Palate Craniofac J; 1995 Jul; 32(4):334-45. PubMed ID: 7548108
[TBL] [Abstract][Full Text] [Related]
16. The vesicular forebrain (pseudo-aprosencephaly): a missing link in the teratogenetic spectrum of the defective brain anlage and its discrimination from aprosencephaly.
Sergi C; Schmitt HP
Acta Neuropathol; 2000 Mar; 99(3):277-84. PubMed ID: 10663970
[TBL] [Abstract][Full Text] [Related]
17. Transposition of the external genitalia associated with caudal regression.
Lage JM; Driscoll SG; Bieber FR
J Urol; 1987 Aug; 138(2):387-9. PubMed ID: 3599260
[TBL] [Abstract][Full Text] [Related]
18. Clinical variability in cerebro-oculo-nasal syndrome: report on two additional cases.
Guion-Almeida ML; Kokitsu-Nakata NM; Richieri-Costa A
Clin Dysmorphol; 2000 Oct; 9(4):253-7. PubMed ID: 11045580
[TBL] [Abstract][Full Text] [Related]
19. Chondrodysplasia, situs inversus totalis, cleft epiglottis and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/absence, micropenis and ambiguous genitalia, imperforate anus.
Fraser FC; Jequier S; Chen MF
Am J Med Genet; 1989 Nov; 34(3):401-5. PubMed ID: 2596528
[No Abstract] [Full Text] [Related]
20. The XK-aprosencephaly syndrome.
Lurie IW; Nedzed MK; Lazjuk GI; Kirillova IA; Cherstvoy ED; Ostrovskaja TI; Shved IA
Am J Med Genet; 1980; 7(2):231-4. PubMed ID: 7193413
[No Abstract] [Full Text] [Related]
[Next] [New Search]