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 *

97 related articles for article (PubMed ID: 31588525)

  • 1. Brief Description of Inheritance Patterns.
    Kövesdi A; Patócs A
    Exp Suppl; 2019; 111():21-27. PubMed ID: 31588525
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Primer in Genetics and Genomics, Article 4-Inheritance Patterns.
    Aiello LB; Chiatti BD
    Biol Res Nurs; 2017 Jul; 19(4):465-472. PubMed ID: 28532160
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics of neurocutaneous disorders: basic principles of inheritance as they apply to neurocutaneous syndromes.
    Dies KA; Sahin M
    Handb Clin Neurol; 2015; 132():3-8. PubMed ID: 26564068
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Somatic and germline mosaicism for a mutation of the PHEX gene can lead to genetic transmission of X-linked hypophosphatemic rickets that mimics an autosomal dominant trait.
    Goji K; Ozaki K; Sadewa AH; Nishio H; Matsuo M
    J Clin Endocrinol Metab; 2006 Feb; 91(2):365-70. PubMed ID: 16303832
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.
    Liu XR; Wu M; He N; Meng H; Wen L; Wang JL; Zhang MP; Li WB; Mao X; Qin JM; Li BM; Tang B; Deng YH; Shi YW; Su T; Yi YH; Tang BS; Liao WP
    Genes Brain Behav; 2013 Mar; 12(2):234-40. PubMed ID: 23190448
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A unique case series of autosomal recessive bestrophinopathy exhibiting multigenerational inheritance.
    Hardin JS; Schaefer GB; Sallam AB; Williams MK; Uwaydat S
    Ophthalmic Genet; 2017 Dec; 38(6):570-574. PubMed ID: 28481155
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heritable one-hit events defining cancer prevention?
    Kopelovich L; Shea-Herbert B
    Cell Cycle; 2013 Aug; 12(16):2553-7. PubMed ID: 23907126
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Malformations among 289,365 Births Attributed to Mutations with Autosomal Dominant and Recessive and X-Linked Inheritance.
    Toufaily MH; Westgate MN; Nasri H; Holmes LB
    Birth Defects Res; 2018 Jan; 110(2):92-97. PubMed ID: 29377642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pseudodominant inheritance pattern in a family with CMT2 caused by GDAP1 mutations.
    van Paassen BW; Bronk M; Verhamme C; van Ruissen F; Baas F; van Spaendonck-Zwarts KY; de Visser M
    J Peripher Nerv Syst; 2017 Dec; 22(4):464-467. PubMed ID: 28837237
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-phenotype correlation in FMF patients: A "non classic" recessive autosomal or "atypical" dominant autosomal inheritance?
    Procopio V; Manti S; Bianco G; Conti G; Romeo A; Maimone F; Arrigo T; Cutrupi MC; Salpietro C; Cuppari C
    Gene; 2018 Jan; 641():279-286. PubMed ID: 29080837
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A somatic and germline mosaic mutation in MPZ/P(0) mimics recessive inheritance of CMT1B.
    Fabrizi GM; Ferrarini M; Cavallaro T; Jarre L; Polo A; Rizzuto N
    Neurology; 2001 Jul; 57(1):101-5. PubMed ID: 11445635
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Germline, hematopoietic, mosaic, and somatic variation: interplay between inherited and acquired genetic alterations in disease assessment.
    Konnick EQ; Pritchard CC
    Genome Med; 2016 Oct; 8(1):100. PubMed ID: 27716394
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK
    Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pseudodominant inheritance in a family with nonautoimmune hypothyroidism due to biallelic DUOX2 mutations.
    Abe K; Narumi S; Suwanai AS; Hamajima T; Hasegawa T
    Clin Endocrinol (Oxf); 2015 Sep; 83(3):394-8. PubMed ID: 25263060
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distinct mutations with different inheritance mode caused similar retinal dystrophies in one family: a demonstration of the importance of genetic annotations in complicated pedigrees.
    Chen X; Sheng X; Liu Y; Li Z; Sun X; Jiang C; Qi R; Yuan S; Wang X; Zhou G; Zhen Y; Xie P; Liu Q; Yan B; Zhao C
    J Transl Med; 2018 May; 16(1):145. PubMed ID: 29843741
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.
    Marx SJ; Agarwal SK; Kester MB; Heppner C; Kim YS; Skarulis MC; James LA; Goldsmith PK; Saggar SK; Park SY; Spiegel AM; Burns AL; Debelenko LV; Zhuang Z; Lubensky IA; Liotta LA; Emmert-Buck MR; Guru SC; Manickam P; Crabtree J; Erdos MR; Collins FS; Chandrasekharappa SC
    Recent Prog Horm Res; 1999; 54():397-438; discussion 438-9. PubMed ID: 10548885
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode.
    Bitner H; Mizrahi-Meissonnier L; Griefner G; Erdinest I; Sharon D; Banin E
    Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5332-8. PubMed ID: 21467170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dominant versus recessive: molecular mechanisms in metabolic disease.
    Zschocke J
    J Inherit Metab Dis; 2008 Oct; 31(5):599-618. PubMed ID: 18932014
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant transmission of complicated hereditary spastic paraplegia due to a dominant negative mutation of KIF1A, SPG30 gene.
    Cheon CK; Lim SH; Kim YM; Kim D; Lee NY; Yoon TS; Kim NS; Kim E; Lee JR
    Sci Rep; 2017 Oct; 7(1):12527. PubMed ID: 28970574
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease.
    Koptides M; Mean R; Demetriou K; Pierides A; Deltas CC
    Hum Mol Genet; 2000 Feb; 9(3):447-52. PubMed ID: 10655555
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.