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 *

192 related articles for article (PubMed ID: 16007635)

  • 41. Assisted Reproductive Technology Surveillance - 
United States, 2013.
    Sunderam S; Kissin DM; Crawford SB; Folger SG; Jamieson DJ; Warner L; Barfield WD;
    MMWR Surveill Summ; 2015 Dec; 64(11):1-25. PubMed ID: 26633040
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Anophthalmia-microphthalmia-oblique clefting syndrome: confirmation of the Fryns anophthalmia syndrome.
    Warburg M; Jensen H; Prause JU; Bolund S; Skovby F; Miranda MJ
    Am J Med Genet; 1997 Nov; 73(1):36-40. PubMed ID: 9375920
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Epidemiologic characteristics of phenotypically distinct neural tube defects among 0.7 million California births, 1983-1987.
    Shaw GM; Jensvold NG; Wasserman CR; Lammer EJ
    Teratology; 1994 Feb; 49(2):143-9. PubMed ID: 8016745
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Congenital malformations co-occurring with hypospadias in California, 1983-1997.
    Yang W; Carmichael SL; Shaw GM
    Am J Med Genet A; 2007 Nov; 143A(22):2627-34. PubMed ID: 17937439
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia.
    Vidya NG; Rajkumar S; Vasavada AR
    Ophthalmic Genet; 2018 Jun; 39(3):344-352. PubMed ID: 29461140
    [TBL] [Abstract][Full Text] [Related]  

  • 46. SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions.
    Bakrania P; Robinson DO; Bunyan DJ; Salt A; Martin A; Crolla JA; Wyatt A; Fielder A; Ainsworth J; Moore A; Read S; Uddin J; Laws D; Pascuel-Salcedo D; Ayuso C; Allen L; Collin JR; Ragge NK
    Br J Ophthalmol; 2007 Nov; 91(11):1471-6. PubMed ID: 17522144
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Assisted reproductive technology surveillance--United States, 2011.
    Sunderam S; Kissin DM; Crawford SB; Folger SG; Jamieson DJ; Barfield WD;
    MMWR Surveill Summ; 2014 Nov; 63(10):1-28. PubMed ID: 25412164
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Anophthalmia and microphthalmia in children: associated ocular, somatic and genetic morbidities and quality of life.
    Fahnehjelm C; Dafgård Kopp E; Wincent J; Güven E; Nilsson M; Olsson M; Teär Fahnehjelm K
    Ophthalmic Genet; 2022 Apr; 43(2):172-183. PubMed ID: 35105264
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A practical guide to the management of anophthalmia and microphthalmia.
    Ragge NK; Subak-Sharpe ID; Collin JR
    Eye (Lond); 2007 Oct; 21(10):1290-300. PubMed ID: 17914432
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing.
    Matías-Pérez D; García-Montaño LA; Cruz-Aguilar M; García-Montalvo IA; Nava-Valdéz J; Barragán-Arevalo T; Villanueva-Mendoza C; Villarroel CE; Guadarrama-Vallejo C; la Cruz RV; Chacón-Camacho O; Zenteno JC
    J Hum Genet; 2018 Nov; 63(11):1169-1180. PubMed ID: 30181649
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Clinical anophthalmia: an epidemiological study in northeast Italy based on 368,256 consecutive births.
    Clementi M; Turolla L; Mammi I; Tenconi R
    Teratology; 1992 Dec; 46(6):551-3. PubMed ID: 1290155
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.
    Marcadier JL; Mears AJ; Woods EA; Fisher J; Airheart C; Qin W; Beaulieu CL; Dyment DA; Innes AM; Curry CJ;
    Am J Med Genet A; 2016 Jan; 170A(1):11-8. PubMed ID: 26373900
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Review of 37 patients with SOX2 pathogenic variants collected by the Anophthalmia/Microphthalmia Clinical Registry and DNA research study.
    Amlie-Wolf L; Bardakjian T; Kopinsky SM; Reis LM; Semina EV; Schneider A
    Am J Med Genet A; 2022 Jan; 188(1):187-198. PubMed ID: 34562068
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Anophthalmia/micro-ophthalmia in syndromes: epidemiology study of newborns in Spain].
    Bermejo Sánchez E; Ayala Garcés A; Félix Rodríguez V; Martín Bermejo M; Blanco García M; Egüés Jimeno J; Huertas Camacho H; Jiménez Muñoz-Delgado N; Paisán Grisolía L; Martínez-Frías ML
    An Esp Pediatr; 1996 Sep; 45(3):269-75. PubMed ID: 9019968
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Assisted Reproductive Technology Surveillance — United States, 2012.
    Sunderam S; Kissin DM; Crawford SB; Folger SG; Jamieson DJ; Warner L; Barfield WD;
    MMWR Surveill Summ; 2015 Aug; 64(6):1-29. PubMed ID: 26270152
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia.
    Habibi I; Youssef M; Marzouk E; El Shakankiri N; Gawdat G; El Sada M; F Schorderet D; Abou Zeid H
    Adv Exp Med Biol; 2019; 1185():221-226. PubMed ID: 31884615
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Congenital bilateral severe microphthalmia with mental retardation and cerebral palsy: chromosome aberration, 46, XY, t (2;6)(q31;q24).
    Hirayama T; Kobayashi T; Fujino O
    J Nippon Med Sch; 2005 Aug; 72(4):242-4. PubMed ID: 16113496
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A novel heterozygous SOX2 mutation causing anophthalmia/microphthalmia with genital anomalies.
    Pedace L; Castori M; Binni F; Pingi A; Grammatico B; Scommegna S; Majore S; Grammatico P
    Eur J Med Genet; 2009; 52(4):273-6. PubMed ID: 19254784
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Clusters of anophthalmia. No link with benomyl in Italy..
    Bianchi F; Calabro A; Calzolari E; Mastroiacovo PP; Petrelli G; Spagnolo A; Tenconi R
    BMJ; 1994 Jan; 308(6922):205. PubMed ID: 8312793
    [No Abstract]   [Full Text] [Related]  

  • 60. Microphthalmia Syndrome 9: Case Report of a Newborn Baby with Pulmonary Hypoplasia, Diaphragmatic Eventration, Microphthalmia, Cardiac Defect and Severe Primary Pulmonary Hypertension.
    Andijani AA; Shajira ES; Abushaheen A; Al-Matary A
    Am J Case Rep; 2019 Mar; 20():354-360. PubMed ID: 30880327
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.