192 related articles for article (PubMed ID: 16155570)
1. Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.
Tischfield MA; Bosley TM; Salih MA; Alorainy IA; Sener EC; Nester MJ; Oystreck DT; Chan WM; Andrews C; Erickson RP; Engle EC
Nat Genet; 2005 Oct; 37(10):1035-7. PubMed ID: 16155570
[TBL] [Abstract][Full Text] [Related]
2. Clinical characterization of the HOXA1 syndrome BSAS variant.
Bosley TM; Salih MA; Alorainy IA; Oystreck DT; Nester M; Abu-Amero KK; Tischfield MA; Engle EC
Neurology; 2007 Sep; 69(12):1245-53. PubMed ID: 17875913
[TBL] [Abstract][Full Text] [Related]
3. The clinical spectrum of homozygous HOXA1 mutations.
Bosley TM; Alorainy IA; Salih MA; Aldhalaan HM; Abu-Amero KK; Oystreck DT; Tischfield MA; Engle EC; Erickson RP
Am J Med Genet A; 2008 May; 146A(10):1235-40. PubMed ID: 18412118
[TBL] [Abstract][Full Text] [Related]
4. Bosley-Salih-Alorainy syndrome in patients from India.
Patil SJ; Karthik GA; Bhavani GS; Bhat V; Matalia J; Shah J; Shukla A; Girisha KM
Am J Med Genet A; 2020 Nov; 182(11):2699-2703. PubMed ID: 32864817
[TBL] [Abstract][Full Text] [Related]
5. Bilateral complete labyrinthine aplasia with bilateral internal carotid artery aplasia, developmental delay, and gaze abnormalities: a presumptive case of a rare HOXA1 mutation syndrome.
Higley MJ; Walkiewicz TW; Miller JH; Curran JG; Towbin RB
AJNR Am J Neuroradiol; 2011 Feb; 32(2):E23-5. PubMed ID: 20075099
[TBL] [Abstract][Full Text] [Related]
6. Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.
Abu-Amero KK; Kondkar AA; Salih MA; Alorainy IA; Khan AO; Oystreck DT; Bosley TM
Ophthalmic Genet; 2013; 34(1-2):90-6. PubMed ID: 22950449
[TBL] [Abstract][Full Text] [Related]
7. HOXA1 mutations are not a common cause of Möbius syndrome.
Rankin JK; Andrews C; Chan WM; Engle EC
J AAPOS; 2010 Feb; 14(1):78-80. PubMed ID: 20227628
[TBL] [Abstract][Full Text] [Related]
8. Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders.
Ingram JL; Stodgell CJ; Hyman SL; Figlewicz DA; Weitkamp LR; Rodier PM
Teratology; 2000 Dec; 62(6):393-405. PubMed ID: 11091361
[TBL] [Abstract][Full Text] [Related]
9. HOXA1 Mutations are Not Commonly Associated with Non-Syndromic Deafness.
Abu-Amero KK; Hagr Aa; Almomani MO; Azad TA; Alorainy IA; Oystreck DT; Bosley TM
Can J Neurol Sci; 2014 Jul; 41(4):448-51. PubMed ID: 24878468
[TBL] [Abstract][Full Text] [Related]
10. Athabascan brainstem dysgenesis syndrome.
Holve S; Friedman B; Hoyme HE; Tarby TJ; Johnstone SJ; Erickson RP; Clericuzio CL; Cunniff C
Am J Med Genet A; 2003 Jul; 120A(2):169-73. PubMed ID: 12833395
[TBL] [Abstract][Full Text] [Related]
11. Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients.
Romano V; Calì F; Mirisola M; Gambino G; D' Anna R; Di Rosa P; Seidita G; Chiavetta V; Aiello F; Canziani F; De Leo G; Ayala GF; Elia M
Mol Psychiatry; 2003 Aug; 8(8):716-7. PubMed ID: 12888798
[No Abstract] [Full Text] [Related]
12. Cardiovascular defects in a mouse model of HOXA1 syndrome.
Makki N; Capecchi MR
Hum Mol Genet; 2012 Jan; 21(1):26-31. PubMed ID: 21940751
[TBL] [Abstract][Full Text] [Related]
13. DYRK1A mutations in two unrelated patients.
Ruaud L; Mignot C; Guët A; Ohl C; Nava C; Héron D; Keren B; Depienne C; Benoit V; Maystadt I; Lederer D; Amsallem D; Piard J
Eur J Med Genet; 2015 Mar; 58(3):168-74. PubMed ID: 25641759
[TBL] [Abstract][Full Text] [Related]
14. Oculomotility disorders arising from disruptions in brainstem motor neuron development.
Engle EC
Arch Neurol; 2007 May; 64(5):633-7. PubMed ID: 17502461
[TBL] [Abstract][Full Text] [Related]
15. Hoxa1 lineage tracing indicates a direct role for Hoxa1 in the development of the inner ear, the heart, and the third rhombomere.
Makki N; Capecchi MR
Dev Biol; 2010 May; 341(2):499-509. PubMed ID: 20171203
[TBL] [Abstract][Full Text] [Related]
16. Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population.
Sen B; Sinha S; Ahmed S; Ghosh S; Gangopadhyay PK; Usha R
Psychiatr Genet; 2007 Feb; 17(1):1. PubMed ID: 17167333
[No Abstract] [Full Text] [Related]
17. No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
Devlin B; Bennett P; Cook EH; Dawson G; Gonen D; Grigorenko EL; McMahon W; Pauls D; Smith M; Spence MA; Schellenberg GD;
Am J Med Genet; 2002 Aug; 114(6):667-72. PubMed ID: 12210285
[TBL] [Abstract][Full Text] [Related]
18. No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD).
Talebizadeh Z; Bittel DC; Miles JH; Takahashi N; Wang CH; Kibiryeva N; Butler MG
J Med Genet; 2002 Nov; 39(11):e70. PubMed ID: 12414832
[No Abstract] [Full Text] [Related]
19. Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.
Rafiq MA; Leblond CS; Saqib MA; Vincent AK; Ambalavanan A; Khan FS; Ayaz M; Shaheen N; Spiegelman D; Ali G; Amin-ud-Din M; Laurent S; Mahmood H; Christian M; Ali N; Fennell A; Nanjiani Z; Egger G; Caron C; Waqas A; Ayub M; Rasheed S; Forgeot d'Arc B; Johnson A; So J; Brohi MQ; Mottron L; Ansar M; Vincent JB; Xiong L
BMC Med Genet; 2015 Jun; 16():41. PubMed ID: 26104215
[TBL] [Abstract][Full Text] [Related]
20. Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?
Makrythanasis P; Gimelli S; Béna F; Dahoun S; Morris MA; Antonarakis SE; Bottani A
Eur J Med Genet; 2012 Jan; 55(1):63-6. PubMed ID: 22080113
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
