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 *

158 related articles for article (PubMed ID: 38380230)

  • 21. Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia.
    Zou Z; Huang L; Lin S; He Z; Zhu H; Zhang Y; Fang Q; Luo Y
    Prenat Diagn; 2018 Jan; 38(2):91-98. PubMed ID: 29171036
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An emerging phenotype of interstitial 15q25.2 microdeletions: clinical report and review.
    Palumbo O; Palumbo P; Palladino T; Stallone R; Miroballo M; Piemontese MR; Zelante L; Carella M
    Am J Med Genet A; 2012 Dec; 158A(12):3182-9. PubMed ID: 23166063
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders.
    Ceylan AC; Citli S; Erdem HB; Sahin I; Acar Arslan E; Erdogan M
    Mol Cytogenet; 2018; 11():54. PubMed ID: 30258496
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The phenotypic spectrum of terminal 6q deletions based on a large cohort derived from social media and literature: a prominent role for DLL1.
    Engwerda A; Kerstjens-Frederikse WS; Corsten-Janssen N; Dijkhuizen T; van Ravenswaaij-Arts CMA
    Orphanet J Rare Dis; 2023 Mar; 18(1):59. PubMed ID: 36935482
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Interstitial deletions in the proximal regions of 6q: 12 original cases and a literature review.
    Machida O; Shimojima KY; Shiihara T; Akamine S; Kira R; Hasegawa Y; Nishi E; Okamoto N; Nagata S; Yamamoto T
    Intractable Rare Dis Res; 2022 Aug; 11(3):143-148. PubMed ID: 36200032
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism.
    Del Refugio Rivera-Vega M; Gómez-Del Angel LA; Valdes-Miranda JM; Pérez-Cabrera A; Gonzalez-Huerta LM; Toral-López J; Cuevas-Covarrubias S
    Cytogenet Genome Res; 2015; 145(1):1-5. PubMed ID: 25870946
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
    Caliebe A; Kroes HY; van der Smagt JJ; Martin-Subero JI; Tönnies H; van 't Slot R; Nievelstein RA; Muhle H; Stephani U; Alfke K; Stefanova I; Hellenbroich Y; Gillessen-Kaesbach G; Hochstenbach R; Siebert R; Poot M
    Eur J Med Genet; 2010; 53(4):179-85. PubMed ID: 20382278
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders.
    Palumbo O; Accadia M; Palumbo P; Leone MP; Scorrano A; Palladino T; Stallone R; Bonaglia MC; Carella M
    Eur J Med Genet; 2018 May; 61(5):248-252. PubMed ID: 29274487
    [TBL] [Abstract][Full Text] [Related]  

  • 29. de novo interstitial deletions at the 11q23.3-q24.2 region.
    Su J; Chen R; Luo J; Fan X; Fu C; Wang J; He S; Hu X; Zhang S; Yi S; Chen S; Shen Y
    Mol Cytogenet; 2016; 9():39. PubMed ID: 27158264
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.
    Tyson C; Qiao Y; Harvard C; Liu X; Bernier FP; McGillivray B; Farrell SA; Arbour L; Chudley AE; Clarke L; Gibson W; Dyack S; McLeod R; Costa T; Vanallen MI; Yong SL; Graham GE; Macleod P; Patel MS; Hurlburt J; Holden JJ; Lewis SM; Rajcan-Separovic E
    Mol Cytogenet; 2008 Nov; 1():23. PubMed ID: 19000322
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A new case of de novo 19p13.2p13.12 deletion in a girl with overgrowth and severe developmental delay.
    Natiq A; Elalaoui SC; Miesch S; Bonnet C; Jonveaux P; Amzazi S; Sefiani A
    Mol Cytogenet; 2014; 7():40. PubMed ID: 24963350
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilaris.
    Al-Maawali A; Marshall CR; Scherer SW; Dupuis L; Mendoza-Londono R; Stavropoulos DJ
    Am J Med Genet A; 2014 Mar; 164A(3):796-800. PubMed ID: 24375972
    [TBL] [Abstract][Full Text] [Related]  

  • 33. De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay.
    Piovani G; Savio G; Traversa M; Pilotta A; De Petro G; Barlati S; Magri C
    Mol Cytogenet; 2014; 7():25. PubMed ID: 24735523
    [TBL] [Abstract][Full Text] [Related]  

  • 34. De Novo 1.77-Mb Microdeletion of 10q22.2q22.3 in a Girl With Developmental Delay, Speech Delay, Congenital Cleft Palate, and Bilateral Hearing Impairment.
    Lei TY; Wang HT; Li F; Cui YQ; Fu F; Li R; Liao C
    Cleft Palate Craniofac J; 2017 May; 54(3):343-350. PubMed ID: 27031267
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Five patients with novel overlapping interstitial deletions in 8q22.2q22.3.
    Kuechler A; Buysse K; Clayton-Smith J; Le Caignec C; David A; Engels H; Kohlhase J; Mari F; Mortier G; Renieri A; Wieczorek D
    Am J Med Genet A; 2011 Aug; 155A(8):1857-64. PubMed ID: 21739578
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Proximal Deletion of 6q Overlapping with Toriello-Carey Facial Phenotype: Prenatal Findings, Clinical Course, Differential Diagnosis, and Review.
    Catena S; Aracena M; Pizarro Ó; Espinoza K; Lay-Son G
    Mol Syndromol; 2017 Dec; 9(1):15-21. PubMed ID: 29456478
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search.
    Vrachnis N; Papoulidis I; Vrachnis D; Siomou E; Antonakopoulos N; Oikonomou S; Zygouris D; Loukas N; Iliodromiti Z; Pavlidou E; Thomaidis L; Manolakos E
    Mol Cytogenet; 2021 Jul; 14(1):39. PubMed ID: 34303382
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.
    Nolen LD; Amor D; Haywood A; St Heaps L; Willcock C; Mihelec M; Tam P; Billson F; Grigg J; Peters G; Jamieson RV
    Am J Med Genet A; 2006 Aug; 140(16):1711-8. PubMed ID: 16835935
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies-Expanding the Phenotype.
    Almoosawy N; Albaghli F; Al-Balool HH; Fathi H; Zakaria WA; Ayed M; Alsharhan H
    Genes (Basel); 2023 Jun; 14(6):. PubMed ID: 37372405
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder.
    Meza-Espinoza JP; Contreras-Gutiérrez JA; Arámbula-Meraz E; González-García JR; Domínguez-Quezada MG; García-Magallanes N; Madueña-Molina J; Benítez-Pascual J; Partida-Pérez M; Picos-Cárdenas VJ
    Mol Cytogenet; 2021 Sep; 14(1):43. PubMed ID: 34481514
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.