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 *

69 related articles for article (PubMed ID: 4383414)

  • 21. [De Lange syndrome].
    Gierowska H; Sobieszczańska L; Miesowicz I
    Wiad Lek; 1970 May; 23(9):773-80. PubMed ID: 5455465
    [No Abstract]   [Full Text] [Related]  

  • 22. Congenital emphysema, cryptorchidism, penoscrotal web, deafness, and mental retardation--a new syndrome?
    Lynch SA; Bushby KM
    Clin Dysmorphol; 1997 Jan; 6(1):35-7. PubMed ID: 9018416
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases].
    Campistol Plana J; Arellano Pedrola M; Poo Argüelles P; Escofet Sotera C; Pérez Olarte P; Vilaseca Buscà MA
    An Esp Pediatr; 1999 Aug; 51(2):139-42. PubMed ID: 10495499
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation).
    Jancar J
    J Ment Defic Res; 1971 Mar; 15(1):20-9. PubMed ID: 5581387
    [No Abstract]   [Full Text] [Related]  

  • 25. A syndrome of retarded development with characteristic appearance.
    Coffin GS
    Am J Dis Child; 1968 Jun; 115(6):698-702. PubMed ID: 4297583
    [No Abstract]   [Full Text] [Related]  

  • 26. Seizure disorder, mental retardation, unusual facies, and abnormal hair.
    Coleman M; Randall J
    J Clin Dysmorphol; 1983; 1(3):28-9. PubMed ID: 6423779
    [No Abstract]   [Full Text] [Related]  

  • 27. [Weaver syndrome. Apropos of a case].
    Alvarez-Coca J; Fullana A; Morena V; Gonzalez M; Oliver A; Gracia R; Peralta A
    An Esp Pediatr; 1984 Oct; 21(6):626-8. PubMed ID: 6524773
    [No Abstract]   [Full Text] [Related]  

  • 28. [A study of the development of bone: II. Percentage estimation of bone age (author's transl)].
    Li GZ
    Zhonghua Fang She Xue Za Zhi; 1979; 13(1):19-23. PubMed ID: 233080
    [No Abstract]   [Full Text] [Related]  

  • 29. Cornelia de Lange syndrome.
    Say B; Balci S; Atasu M
    Turk J Pediatr; 1969 Oct; 11(4):166-80. PubMed ID: 5402549
    [No Abstract]   [Full Text] [Related]  

  • 30. [Rubinstein-Taybi syndrome. Combined development-stimulating therapy].
    Wittrock J; Schmitz E
    Fortschr Med; 1973 Nov; 91(32):1272-8. PubMed ID: 4751355
    [No Abstract]   [Full Text] [Related]  

  • 31. Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome.
    Majewski F; Goecke T
    Am J Med Genet; 1982 May; 12(1):7-21. PubMed ID: 7046443
    [No Abstract]   [Full Text] [Related]  

  • 32. Cohen syndrome: further delineation and inheritance.
    Kousseff BG
    Am J Med Genet; 1981; 9(1):25-30. PubMed ID: 7246618
    [TBL] [Abstract][Full Text] [Related]  

  • 33. MCA/MR syndrome with severe pre- and postnatal growth retardation, deep mental retardation, distinct facial appearance with nasal hypoplasia, cleft palate and retino-choroidal coloboma in two unrelated female patients.
    Fryns JP
    Genet Couns; 2000; 11(4):399-402. PubMed ID: 11140419
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The clinical course of mannosidosis.
    Autio S; Louhimo T; Helenius M
    Ann Clin Res; 1982 Apr; 14(2):93-7. PubMed ID: 7149616
    [TBL] [Abstract][Full Text] [Related]  

  • 35. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
    Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
    BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Neonatal seizures with tonic clonic sequences and poor developmental outcome.
    Schmitt B; Wohlrab G; Sander T; Steinlein OK; Hajnal BL
    Epilepsy Res; 2005 Jul; 65(3):161-8. PubMed ID: 16039833
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Epilepsy in childhood. Studies on material of a pediatric university clinic during a decade].
    Stögmann W
    Wien Med Wochenschr; 1969 Dec; 119(49):845-9. PubMed ID: 4989194
    [No Abstract]   [Full Text] [Related]  

  • 38. A variant example of familial Floating-Harbor syndrome?
    Peñaloza JM; García-Cruz D; Dávalos IP; Dávalos NO; García-Cruz MO; Pérez-Rulfo D; Sánchez-Corona J
    Genet Couns; 2003; 14(1):31-7. PubMed ID: 12725587
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Völkl TM; Simm D; Beier C; Dörr HG
    Pediatrics; 2006 Jan; 117(1):e98-105. PubMed ID: 16396852
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
    D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
    Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.