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 *

257 related articles for article (PubMed ID: 8031542)

  • 1. LADD syndrome in five members of a three-generation family and prenatal diagnosis.
    Francannet C; Vanlieferinghen P; Dechelotte P; Urbain MF; Campagne D; Malpuech G
    Genet Couns; 1994; 5(1):85-91. PubMed ID: 8031542
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lacrimo-auriculo-dento-digital syndrome: a literature review and case reports.
    Toumba KJ; Gutteridge DL
    Quintessence Int; 1995 Dec; 26(12):829-39. PubMed ID: 8596813
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lacrimo-auriculo-dento-digital syndrome: evidence for lower limb involvement and severe congenital renal anomalies.
    Bamforth JS; Kaurah P
    Am J Med Genet; 1992 Aug; 43(6):932-7. PubMed ID: 1415342
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome.
    Horn D; Witkowski R
    Genet Couns; 1993; 4(4):305-9. PubMed ID: 8110420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The lacrimo-auriculo-dento-digital syndrome.
    Shiang EL; Holmes LB
    Pediatrics; 1977 Jun; 59(6):927-30. PubMed ID: 865946
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lacrimo-auriculo-dento-digital (LADD) syndrome.
    Hollister DW; Klein SH; de Jager HJ; Lachman RS; Rimoin DL
    Birth Defects Orig Artic Ser; 1974; 10(5):153-66. PubMed ID: 4469979
    [No Abstract]   [Full Text] [Related]  

  • 7. [Clinical diagnosis of familial Levy-Hollister syndrome].
    Vila Pérez D; Palanca Arias D; Gean Molins E; Palomeque Rico A
    An Pediatr (Barc); 2014 Feb; 80(2):114-6. PubMed ID: 23562527
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Orodental findings of a family with lacrimo-auriculo-dento digital (LADD) syndrome.
    Guven Y; Rosti RO; Tuna EB; Kayserili H; Aktoren O
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Dec; 106(6):e33-44. PubMed ID: 18801668
    [TBL] [Abstract][Full Text] [Related]  

  • 9. LADD syndrome is caused by FGF10 mutations.
    Milunsky JM; Zhao G; Maher TA; Colby R; Everman DB
    Clin Genet; 2006 Apr; 69(4):349-54. PubMed ID: 16630169
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP; Moerman P
    Genet Couns; 1998; 9(1):61-2. PubMed ID: 9555592
    [No Abstract]   [Full Text] [Related]  

  • 11. [Diagnosis of familial Holt-Oram syndrome].
    Lehner R; Wenzl R; Vanura H; Frank W; Safar P; Husslein P
    Z Geburtshilfe Perinatol; 1994 Aug; 198(4):143-9. PubMed ID: 7975801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestations.
    Robins DB; Ladda RL; Thieme GA; Boal DK; Emanuel BS; Zackai EH
    Am J Med Genet; 1989 Mar; 32(3):390-4. PubMed ID: 2658590
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The lacrimo-auriculo-dento-digital syndrome.
    Hollister DW; Klein SH; De Jager HJ; Lachman RS; Rimoin DL
    J Pediatr; 1973 Sep; 83(3):438-44. PubMed ID: 4725147
    [No Abstract]   [Full Text] [Related]  

  • 14. Lacrimo-auriculo-dento-digital syndrome. Case report, review of the literature, and clinical spectrum.
    Lehotay M; Kunkel M; Wehrbein H
    J Orofac Orthop; 2004 Sep; 65(5):425-32. PubMed ID: 15378197
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
    Amador C; Mathews AM; Del Carmen Montoya M; Laughridge ME; Everman DB; Holden KR
    J Child Neurol; 2008 Aug; 23(8):901-5. PubMed ID: 18660473
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lacrimo-auriculo-dento-digital syndrome: A novel mutation in a Korean family and review of literature.
    Ryu YH; Kyun Chae J; Kim JW; Lee S
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1412. PubMed ID: 32715658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of a case with anencephaly-omphalocele-unilateral absent radial ray.
    Ceylaner S; Ceylaner G; Altun M; Coşkun A; Danisman N
    Genet Couns; 2009; 20(2):189-93. PubMed ID: 19650417
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dental issues in lacrimo-auriculo-dento-digital syndrome: An autosomal dominant condition with clinical and genetic variability.
    Hajianpour MJ; Bombei H; Lieberman SM; Revell R; Krishna R; Gregorsok R; Kao S; Milunsky JM
    J Am Dent Assoc; 2017 Mar; 148(3):157-163. PubMed ID: 28043400
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lacrimoauriculodentodigital syndrome with cleft lip/palate and renal manifestations.
    Ramirez D; Lammer EJ
    Cleft Palate Craniofac J; 2004 Sep; 41(5):501-6. PubMed ID: 15352854
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations.
    Chen CP; Chern SR; Tsai EJ; Lee CC; Chen LF; Wang W
    Genet Couns; 2009; 20(3):281-8. PubMed ID: 19852436
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.