Alao MJ - Search Results

1

Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imaging.

Alao MJ, Bonneau D, Holder-Espinasse M, Goizet C, Manouvrier-Hanu S, Mezel A, Petit F, Subtil D, Magdelaine C, Lacombe D. Alao MJ, et al. Eur J Med Genet. 2010 Jan-Feb;53(1):19-22. doi: 10.1016/j.ejmg.2009.08.007. Epub 2009 Oct 4. Eur J Med Genet. 2010. PMID: 19808103 Free article.

2

Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female.

Alao MJ, Lalèyè A, Lalya F, Hans Ch, Abramovicz M, Morice-Picard F, Arveiler B, Lacombe D, Rooryck C. Alao MJ, et al. Eur J Med Genet. 2012 Nov;55(11):630-4. doi: 10.1016/j.ejmg.2012.07.005. Epub 2012 Aug 3. Eur J Med Genet. 2012. PMID: 22906557

3

Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African family.

Laleye A, Alao MJ, Gbessi G, Adjagba M, Marche M, Coupry I, Redonnet-Vernhet I, Lepreux S, Ayivi B, Darboux RB, Lacombe D, Arveiler B. Laleye A, et al. Among authors: alao mj. Genet Couns. 2008;19(2):183-92. Genet Couns. 2008. PMID: 18618993

4

Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.

Laleye A, Alao MJ, Adjagba M, Hans C, Delneste D, Gnamey DK, Ayivi B, Darboux RB. Laleye A, et al. Among authors: alao mj. Genet Couns. 2006;17(1):35-40. Genet Couns. 2006. PMID: 16719275

5

Femoral hypoplasia-unusual facies syndrome in a black African infant.

Alao MJ, Gbénou S, Yèkpè P, Laleye A. Alao MJ, et al. Genet Couns. 2011;22(4):365-70. Genet Couns. 2011. PMID: 22303796

6

[Usefulness of neonatal exams at Cotonou University Hospital, Benin].

d'Almeida M, Bagnan L, Alao M, Alihonou F, Ayivi B. d'Almeida M, et al. Among authors: alao m. Mali Med. 2011;26(4):8-11. Mali Med. 2011. PMID: 22765946 French.

7

[Role of severe anemia and hypoglycemia in severe malaria's mortality in children in a pediatric ward in Parakou (Benin)].

Adedemy JD, Agossou J, Alao MJ, Noudamadjo A, Ayivi B. Adedemy JD, et al. Among authors: alao mj. Mali Med. 2015;30(1):19-24. Mali Med. 2015. PMID: 29927153 French.

8

[Pleural effusion in children at the National Hospital Center and University of Cotonou: epidemiological, clinical and therapeutic aspects].

Alao MJ, Sagbo GG, Diakité AA, Ayivi B. Alao MJ, et al. Mali Med. 2010;25(4):47-51. Mali Med. 2010. PMID: 21470942 French.

9

[Profile of HIV-infected children at the National University Hospital of Cotonou (CNHU)].

d'Almeida M, Sagbo G, Lalya F, Alao MJ, d'Almeida C, Agossou J, Koumakpai S, Ayivi B. d'Almeida M, et al. Among authors: alao mj. Mali Med. 2013;28(1):25-29. Mali Med. 2013. PMID: 29925217 French.

10

Primary autosomal recessive microcephaly: a novel clinical phenotype.

Gnamey DK, Alao MJ, Agbodjan-Djossou O, Koffi SK. Gnamey DK, et al. Among authors: alao mj. Genet Couns. 2005;16(1):107-8. Genet Couns. 2005. PMID: 15844788 No abstract available.

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