April 2024
1. VANDEN BROEK K, Ryu JR, Perrier R, Tyndall AV, et al
   SAM domain variants of EPHB4 associated with aberrant signaling are linked to lymphatic-related fetal hydrops and facial dysmorphology.
   Clin Genet. 2024;105:386-396.
   

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   May 2023
2. AL-KOUATLY HB, Shivashankar K, Mossayebi MH, Makhamreh M, et al
   Diagnostic yield from prenatal exome sequencing for non-immune hydrops fetalis: A systematic review and meta-analysis.
   Clin Genet. 2023;103:503-512.
   

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3. GHESH L, Desir J, Haye D, Le Tanno P, et al
   Perinatal presentations of non-immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis.
   Clin Genet. 2023;103:560-565.
   

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   December 2022
4. TAO C, Zhu T, Tang S, Lu J, et al
   Novo pathogenic variations of NLRP7 increasing the risk of gestational trophoblastic neoplasia.
   Clin Genet. 2022 Dec 21. doi: 10.1111/cge.14288.
   

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5. GHESH L, Besnard T, Joubert M, Picard V, et al
   A Gardos channelopathy associated with nonimmune hydrops and fetal loss.
   Clin Genet. 2022;102:543-547.
   

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   November 2022
6. DE FRANCO E, Wakeling MN, Frew RD, Russ-Silsby J, et al
   A biallelic loss-of-function PDIA6 variant in a second patient with polycystic kidney disease, infancy-onset diabetes, and microcephaly.
   Clin Genet. 2022;102:457-458.
   

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   November 2021
7. IYER NS, Gimovsky AC, Ferreira CR, Critchlow E, et al
   Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review.
   Clin Genet. 2021;100:493-503.
   

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   October 2021
8. COUCEIRO J, Matos I, Mendes JJ, Baptista PV, et al
   Inflammatory factors, genetic variants, and predisposition for preterm birth.
   Clin Genet. 2021;100:357-367.
   

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   June 2021
9. REZAEI M, Suresh B, Bereke E, Hadipour Z, et al
   Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.
   Clin Genet. 2021;99:823-828.
   

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   April 2021
10. TABOLACCI E, Molinario C, Marangi G, Nobile V, et al
    Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization.
    Clin Genet. 2021;99:601-603.
    

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    February 2021
11. ZHENG W, Hu H, Dai J, Zhang S, et al
    Expanding the genetic and phenotypic spectrum of the subcortical maternal complex genes in recurrent preimplantation embryonic arrest.
    Clin Genet. 2021;99:286-291.
    

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