These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 30922974)

  • 1. Whole Exome Sequencing Identifies a Rare Nonsense Mutation in FAM47C as a Possible Cause of Severe Oligospermia in Brothers With Varicocele.
    Chertman W; Arora H; Griswold AJ; Lopategui DM; Ramasamy R
    Urology; 2019 Jul; 129():71-73. PubMed ID: 30922974
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.
    Tu C; Meng L; Nie H; Yuan S; Wang W; Du J; Lu G; Lin G; Tan YQ
    Fertil Steril; 2020 Mar; 113(3):561-568. PubMed ID: 32111475
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
    Okutman O; Muller J; Skory V; Garnier JM; Gaucherot A; Baert Y; Lamour V; Serdarogullari M; Gultomruk M; Röpke A; Kliesch S; Herbepin V; Aknin I; Benkhalifa M; Teletin M; Bakircioglu E; Goossens E; Charlet-Berguerand N; Bahceci M; Tüttelmann F; Viville S
    J Assist Reprod Genet; 2017 May; 34(5):683-694. PubMed ID: 28401488
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.
    Li L; Sha YW; Su ZY; Mei LB; Ji ZY; Zhang Q; Lin SB; Wang X; Qiu PP; Li P; Yin C
    Gene; 2018 Jan; 639():106-110. PubMed ID: 29017965
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Y chromosome microdeletions in severe oligospermia men with varicocele].
    Zhu HB; Li LL; Dai RL; Fadlalla E; Li LL; Liu RZ
    Zhonghua Nan Ke Xue; 2012 Nov; 18(11):969-72. PubMed ID: 23214243
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
    Okutman O; Muller J; Baert Y; Serdarogullari M; Gultomruk M; Piton A; Rombaut C; Benkhalifa M; Teletin M; Skory V; Bakircioglu E; Goossens E; Bahceci M; Viville S
    Hum Mol Genet; 2015 Oct; 24(19):5581-8. PubMed ID: 26199321
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndrome.
    Katagiri S; Yoshitake K; Akahori M; Hayashi T; Furuno M; Nishino J; Ikeo K; Tsuneoka H; Iwata T
    Mol Vis; 2013; 19():2393-406. PubMed ID: 24319333
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Azoospermia factor deletions in varicocele cases with severe oligozoospermia.
    Dada R; Kumar R; Shamsi MB; Sidhu T; Mitra A; Singh S; Kumar R; Sharma RS; Gupta SK; Gupta NP
    Indian J Med Sci; 2007 Sep; 61(9):505-10. PubMed ID: 17785886
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
    Kasak L; Punab M; Nagirnaja L; Grigorova M; Minajeva A; Lopes AM; Punab AM; Aston KI; Carvalho F; Laasik E; Smith LB; ; Conrad DF; Laan M
    Am J Hum Genet; 2018 Aug; 103(2):200-212. PubMed ID: 30075111
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Single-Exome sequencing identified a novel RP2 mutation in a child with X-linked retinitis pigmentosa.
    Lim H; Park YM; Lee JK; Taek Lim H
    Can J Ophthalmol; 2016 Oct; 51(5):326-330. PubMed ID: 27769321
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Nonsense Mutation in HOXD13 Gene from A Chinese Family with Non-Syndromic Synpolydactyly.
    Guo X; Shi T; Lin M; Zhang Y
    Tohoku J Exp Med; 2019 Oct; 249(2):93-100. PubMed ID: 31611522
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case study of a patient with cryptozoospermia associated with a recessive
    Wang X; Jin HR; Cui YQ; Chen J; Sha YW; Gao ZL
    Asian J Androl; 2018; 20(1):101-102. PubMed ID: 28303806
    [No Abstract]   [Full Text] [Related]  

  • 13. Varicocele and male infertility in Northeast China: Y chromosome microdeletion as an underlying cause.
    Dai RL; Hou Y; Li FB; Yue JM; Xi Q; Liu RZ
    Genet Mol Res; 2015 Jun; 14(2):6583-90. PubMed ID: 26125865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Case report. Patient with varicocele & oligozoospermia with Y chromosome microdeletion: AZFb+c].
    Meza-Vázquez HE; Rosas-Vargas H; Vite-Velázquez EJ; De Alba-Mayans AG
    Actas Urol Esp; 2007 Mar; 31(3):285-8. PubMed ID: 17658159
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
    Huang H; Chen YQ; Fan LL; Guo S; Li JJ; Jin JY; Xiang R
    J Cell Mol Med; 2018 Feb; 22(2):1350-1354. PubMed ID: 29077258
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of evidence of a genetic origin in the impaired spermatogenesis of a patient cohort with low-grade varicocele.
    Foppiani L; Cavani S; Piredda S; Perroni L; Fazzuoli L; Giusti M
    J Endocrinol Invest; 2001 Apr; 24(4):217-23. PubMed ID: 11383907
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing.
    Lopategui DM; Griswold AJ; Arora H; Clavijo RI; Tekin M; Ramasamy R
    Andrology; 2018 Jan; 6(1):53-57. PubMed ID: 29211946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole exome sequencing identifies a homozygous nonsense variation in ALMS1 gene in a patient with syndromic obesity.
    Das Bhowmik A; Gupta N; Dalal A; Kabra M
    Obes Res Clin Pract; 2017; 11(2):241-246. PubMed ID: 27665122
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-exome sequencing identified a novel mutation in
    Tang H; Mao J; Xiang J; Liu M; Li H; Wang T
    J Genet; 2021; 100():. PubMed ID: 34282730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Bilateral microsurgical varicocelectomy in infertile men].
    Chovelidze ShG; Tritto J; Getta T
    Urologiia; 2004; (3):21-5. PubMed ID: 15199809
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.