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 *

112 related articles for article (PubMed ID: 11311003)

  • 1. Total anomalous pulmonary venous connection and a constellation of craniofacial, skeletal, and urogenital anomalies in a newborn and similar features in his 36-year-old father.
    Pierson DM; Taboada EM; Lofland GK; Begleiter ML; Smith GS; Hall F; Butler MG
    Clin Dysmorphol; 2001 Apr; 10(2):95-9. PubMed ID: 11311003
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Brachyphalangy, feet polydactyly, absent/hypoplastic tibiae: a further case and review of main diagnostic findings.
    Faravelli F; Di Rocco M; Stella G; Selicorni A; Camera G
    Clin Dysmorphol; 2001 Apr; 10(2):101-3. PubMed ID: 11310988
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A syndrome of brachyphalangy, polydactyly and absent tibiae.
    Baraitser M; Stewart F; Winter RM; Hall CM; Herman S; Nevin NC
    Clin Dysmorphol; 1997 Apr; 6(2):111-21. PubMed ID: 9134290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literature.
    Shafeghati Y; Kahrizi K; Najmabadi H; Kuss AW; Ropers HH; Tzschach A
    Eur J Pediatr; 2010 Dec; 169(12):1535-9. PubMed ID: 20661588
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Additional features in a new case of a girl presenting brachyphalangy, polydactyly and tibial aplasia/hypoplasia.
    Bernardi P; Graziadio C; Rosa RF; Dall'Agnol L; Zen PR; Paskulin GA
    Am J Med Genet A; 2009 Jul; 149A(7):1532-8. PubMed ID: 19533791
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tibial aplasia, lower extremity mirror image polydactyly, brachyphalangy, craniofacial dysmorphism and genital hypoplasia: further delineation and mutational analysis.
    Wechsler SB; Lehoczky JA; Hall JG; Innis JW
    Clin Dysmorphol; 2004 Apr; 13(2):63-69. PubMed ID: 15057119
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Brachycephaly, cutis aplasia congenita, blue sclerae, hypertelorism, polydactyly, hypoplastic nipples, failure to thrive, and developmental delay: a distinct autosomal recessive syndrome?
    Teebi AS; Druker HA
    Clin Dysmorphol; 2001 Jan; 10(1):69-70. PubMed ID: 11152154
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Father and two children with total anomalous pulmonary venous connection.
    Raisher BD; Dowton SB; Grant JW
    Am J Med Genet; 1991 Jul; 40(1):105-6. PubMed ID: 1887837
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tibial hemimelia-polydactyly-five-fingered hand syndrome associated with a 404 G>A mutation in a distant sonic hedgehog cis-regulator (ZRS): a case report.
    Cho TJ; Baek GH; Lee HR; Moon HJ; Yoo WJ; Choi IH
    J Pediatr Orthop B; 2013 May; 22(3):219-21. PubMed ID: 22314436
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hypoplasia of the tibia, polydactyly, and triphalangeal thumb: 1st family described in Venezuela].
    Martínez-Basalo C; González-Inciarte ME; Delgado-Luengo W; Casilla-Nava S; González-Incíarte L; Alvarez-Nava F; Boscán-Porras N; Delgado-Luengo J
    Invest Clin; 1997 Dec; 38(4):219-26. PubMed ID: 9527389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormal facial appearance, body asymmetry, limb deformities, and internal malformations.
    Oudesluijs G; Simon ME; Burggraaf RH; Waterham HR; Hennekam RC
    Am J Med Genet A; 2012 Feb; 158A(2):292-7. PubMed ID: 22140078
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Greig cephalopolysyndactyly syndrome in a family.
    Wang CH; Tsai FJ; Shi YR
    Acta Paediatr Taiwan; 2006; 47(2):95-9. PubMed ID: 16927636
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorder.
    Holmes LB; Redline RW; Brown DL; Williams AJ; Collins T
    J Med Genet; 1995 Nov; 32(11):896-900. PubMed ID: 8592337
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV; Delp K
    Clin Dysmorphol; 1994 Oct; 3(4):335-9. PubMed ID: 7894738
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies.
    Urioste M; Rodríguez JI; Barcia JM; Martín M; Escribá R; Pardo M; Camino J; Martínez-Frías ML
    Am J Med Genet; 1993 Sep; 47(4):494-503. PubMed ID: 8256813
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fraser syndrome with partial anomalous pulmonary venous connection.
    Thapa R; Bhattacharya A
    Indian Pediatr; 2008 Jun; 45(6):510-1. PubMed ID: 18599943
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aplasia of tibia with split-hand/split-foot deformity. Report of six families with 35 cases and considerations about variability and penetrance.
    Majewski F; Küster W; ter Haar B; Goecke T
    Hum Genet; 1985; 70(2):136-47. PubMed ID: 4007857
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypoplastic left heart and postaxial polydactyly.
    Brennan P
    Clin Dysmorphol; 2001 Jul; 10(3):219-22. PubMed ID: 11446418
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A hereditable combination of congenital anomalies.
    Agarwal RP; Jain D; Ramesh Babu CS; Garg RK
    J Bone Joint Surg Br; 1996 May; 78(3):492-4. PubMed ID: 8636194
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.