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2021 | 1 |
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Page 1
The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations.
Front Reprod Health. 2023 Mar 27;5:1132662. doi: 10.3389/frph.2023.1132662. eCollection 2023.
Front Reprod Health. 2023.
PMID: 37050939
Free PMC article.
Childhood Hypophosphatasia Associated with a Novel Biallelic ALPL Variant at the TNSALP Dimer Interface.
Martins L, Lessa LGF, Ali TM, Lazar M, Kim CA, Kantovitz KR, Santamaria MP, Araújo CF, Ramos CJ, Foster BL, Franco JFS, Bertola D, Nociti FH Jr.
Martins L, et al. Among authors: ali tm.
Int J Mol Sci. 2022 Dec 23;24(1):282. doi: 10.3390/ijms24010282.
Int J Mol Sci. 2022.
PMID: 36613725
Free PMC article.
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The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry.
Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Cabral de Menezes Filho H, Kim CA, Bertola DR.
Ali TM, et al.
Am J Med Genet A. 2022 May;188(5):1545-1549. doi: 10.1002/ajmg.a.62651. Epub 2022 Jan 12.
Am J Med Genet A. 2022.
PMID: 35019224
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Balanced chromosomal rearrangement in a partner revealed after Preimplantation Genetic Testing for Aneuploidies (PGT-A).
Ceschin I, Ali TM, Carvalho CV, Martins C, Bos-Mikich A, Andrade GM, Frantz N.
Ceschin I, et al. Among authors: ali tm.
JBRA Assist Reprod. 2023 Feb 7;27(2):320-324. doi: 10.5935/1518-0557.20220058. Online ahead of print.
JBRA Assist Reprod. 2023.
PMID: 36749811
Free PMC article.
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Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report.
Ali TM, Mateu-Brull E, Balaguer N, Dantas C, Borges HR, de Oliveira MQG, Rodrigo L, Campos-Galindo I, Navarro R, Milán M.
Ali TM, et al.
Eur J Med Res. 2021 Jun 29;26(1):64. doi: 10.1186/s40001-021-00535-5.
Eur J Med Res. 2021.
PMID: 34187576
Free PMC article.
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