BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 14571271)

  • 21. Familial Sotos syndrome (cerebral gigantism): craniofacial and psychological characteristics.
    Bale AE; Drum MA; Parry DM; Mulvihill JJ
    Am J Med Genet; 1985 Apr; 20(4):613-24. PubMed ID: 2581446
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome.
    Doerfler W; Wieczorek D; Gillessen-Kaesbach G; Albrecht B; Passarge E
    Am J Med Genet; 1997 Dec; 73(2):210-6. PubMed ID: 9409875
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Lymphoproliferative disorders in Sotos syndrome: observation of two cases.
    Corsello G; Giuffrè M; Carcione A; Cuzto ML; Piccione M; Ziino O
    Am J Med Genet; 1996 Sep; 64(4):588-93. PubMed ID: 8870927
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Niikawa-Kuroki syndrome.
    Roccella M
    Minerva Pediatr; 1999; 51(7-8):271-8. PubMed ID: 10634060
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Deletion of (11)(q24.2) in a mother and daughter with similar phenotypes.
    Neavel CB; Soukup S
    Am J Med Genet; 1994 Dec; 53(4):321-4. PubMed ID: 7864040
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Floating Harbor syndrome. Case report and further syndrome delineation.
    Midro AT; Olchowik B; Rogowska M; Hubert E; Hassman-Poznańska E; Papasz A; Szulc S; Wiśniewski A
    Ann Genet; 1997; 40(3):133-8. PubMed ID: 9401100
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Plantar lipomatosis, unusual facial phenotype and developmental delay: a new MCA/MR syndrome.
    Pierpont ME; Stewart FJ; Gorlin RJ
    Am J Med Genet; 1998 Jan; 75(1):18-21. PubMed ID: 9450851
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A; Seven M; Deviren A; Söylemez MA; Hacihanefioğlu S; Ulutin T; Cenani A
    Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Nonsyndromal overgrowth in males with mild psychomotor delay.
    Neri G; Steindl K; Mazzei A; Battaglia A; Cappa M
    Am J Med Genet; 1998 Oct; 79(4):291-3. PubMed ID: 9781910
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Sotos syndrome and cutis laxa.
    Robertson SP; Bankier A
    J Med Genet; 1999 Jan; 36(1):51-6. PubMed ID: 9950366
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents.
    Vogels A; Devriendt K; Legius E; Decock P; Marien J; Hendrickx G; Fryns JP
    Genet Couns; 1998; 9(4):245-53. PubMed ID: 9894160
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Acrofacial dysostosis with growth and mental retardation in three males, one with simultaneous Hermansky-Pudlak syndrome.
    Kelly TE; Cooke RJ; Kester RW
    Birth Defects Orig Artic Ser; 1977; 13(3B):45-52. PubMed ID: 890099
    [No Abstract]   [Full Text] [Related]  

  • 33. [Sotos syndrome: follow-up of a case with precocious puberty].
    Bertelloni S; Baroncelli GI; Tomasi O; Sorrentino MC; Costa S; Saggese G
    Pediatr Med Chir; 1995; 17(4):353-7. PubMed ID: 7491333
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Changing phenotype in Floating-Harbor syndrome.
    Hersh JH; Groom KR; Yen FF; Verdi GD
    Am J Med Genet; 1998 Feb; 76(1):58-61. PubMed ID: 9508066
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Variability of the Brachmann-de Lange syndrome.
    Selicorni A; Lalatta F; Livini E; Briscioli V; Piguzzi T; Bagozzi DC; Mastroiacovo P; Zampino G; Gaeta G; Pugliese A
    Am J Med Genet; 1993 Nov; 47(7):977-82. PubMed ID: 8291540
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome.
    Calcagni G; Ferrigno F; Franceschini A; Dentici ML; Capolino R; Sinibaldi L; Minotti C; Micalizzi A; Alesi V; Novelli A; Baban A; Parlapiano G; Coviello D; Versacci P; Putotto C; Chinali M; Drago F; Bartuli A; Marino B; Digilio MC
    Diagnostics (Basel); 2024 Mar; 14(6):. PubMed ID: 38535015
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Sotos syndrome treated with traditional Chinese medicine and rehabilitation: Case report.
    Chen S; Zou P; Ge L; Cheng X
    Medicine (Baltimore); 2023 Dec; 102(48):e36169. PubMed ID: 38050304
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay: a 4p deletion?
    de Die-Smulders C; Schrander-Stumpel C; Fryns JP
    Am J Med Genet; 1993 Nov; 47(6):936. PubMed ID: 7506486
    [No Abstract]   [Full Text] [Related]  

  • 39. A Japanese male infant with the Weaver syndrome.
    Kondo I; Mori Y; Kuwajima K
    Jinrui Idengaku Zasshi; 1990 Sep; 35(3):257-62. PubMed ID: 2266602
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Weaver syndrome: the changing phenotype in an adult.
    Greenberg F; Wasiewski W; McCabe ER
    Am J Med Genet; 1989 May; 33(1):127-9. PubMed ID: 2750780
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.