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 *

120 related articles for article (PubMed ID: 4155966)

  • 21. [Incontinentia pigmenti. Clinical and histological considerations on 2 cases].
    Reboa E; Castellani R; Anselmi L
    Minerva Pediatr; 1969 Feb; 21(7):274-80. PubMed ID: 5821161
    [No Abstract]   [Full Text] [Related]  

  • 22. Prevalence of dental caries in handicapped children of Calcutta.
    Gupta DP; Chowdhury R; Sarkar S
    J Indian Soc Pedod Prev Dent; 1993 Mar; 11(1):23-7. PubMed ID: 8040696
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Report on two patients with Costello syndrome and sialuria.
    Di Rocco M; Gatti R; Gandullia P; Barabino A; Picco P; Borrone C
    Am J Med Genet; 1993 Nov; 47(7):1135-40. PubMed ID: 8291534
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Clinical considerations on a probable new case of the Coffin-Siris syndrome].
    D'Elia R; Cassone L; Senatore A; Scianaro L; Loiodice G
    Minerva Pediatr; 1981 Oct; 33(20):1021-4. PubMed ID: 7311957
    [No Abstract]   [Full Text] [Related]  

  • 25. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family.
    Wulfsberg EA; Campbell AB; Lurie IW; Eanet KR
    Am J Med Genet; 1996 Jun; 63(4):554-7. PubMed ID: 8826434
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Partial trisomy C by t(Cp-; B+) translocation].
    De Grouchy J; Roy C; Lachance R; Frezal J; Lamy M
    Arch Fr Pediatr; 1967 Oct; 24(8):849-58. PubMed ID: 5584188
    [No Abstract]   [Full Text] [Related]  

  • 27. Mental retardation, hypotrichosis and syndactyly: a new entity?
    Lopes VL; Marques-De-Faria AP
    Genet Couns; 1996; 7(1):47-51. PubMed ID: 8652088
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Presentation of a case of an unusual malformative syndrome: the Schönenberg syndrome].
    Buffoni L; Chiossi FM
    Minerva Pediatr; 1971 Sep; 23(38):1549-54. PubMed ID: 4399309
    [No Abstract]   [Full Text] [Related]  

  • 29. [The Rubinstein-Taybi syndrome].
    Petrocini S; Cugini A
    Minerva Pediatr; 1969 Apr; 21(15):624-32. PubMed ID: 5402257
    [No Abstract]   [Full Text] [Related]  

  • 30. [Bazex, Dupré and Christol syndrome. Apropos of a case with prolymphocytic leukemia].
    Colomb D; Ducros B; Boussuge N
    Ann Dermatol Venereol; 1989; 116(5):381-7. PubMed ID: 2675736
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical trichology.
    Bartosová L; St'áva Z; Jorda V
    Curr Probl Dermatol; 1984; 12():59-184. PubMed ID: 6238807
    [No Abstract]   [Full Text] [Related]  

  • 32. Pigmentary changes and atopic dermatitis in a patient with Seckel syndrome.
    Brackeen A; Babb-Tarbox M; Smith J
    Pediatr Dermatol; 2007; 24(1):53-6. PubMed ID: 17300651
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Congenital minor anomalies in mentally retarded children.
    Arima M; Komiya K; Ono K; Hisada K
    Proc Aust Assoc Neurol; 1968; 5(1):177-82. PubMed ID: 5709957
    [No Abstract]   [Full Text] [Related]  

  • 34. Skeletal dysplasia, hyperpigmentation, cutis laxa, endocrine abnormality, and mental retardation--the Patterson syndrome.
    David TJ
    Prog Clin Biol Res; 1982; 104():331-7. PubMed ID: 7163277
    [No Abstract]   [Full Text] [Related]  

  • 35. [Coincidence of disorders of hair growth and follicular melanogenesis in various pathological conditions].
    Kostanecki W; Kwiatkowska E; Mazurkiewicz W; Zak R; Bachurzewski J; Skocińska M
    Przegl Dermatol; 1969; 56(2):185-91. PubMed ID: 4239840
    [No Abstract]   [Full Text] [Related]  

  • 36. Alopecia-anosmia-deafness-hypogonadism syndrome revisited: report of a new case.
    Johnston K; Golabi M; Hall B; Ito M; Grix A
    Am J Med Genet; 1987 Apr; 26(4):925-7. PubMed ID: 3591836
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Generalized spiny hyperkeratosis, universal alopecia, and deafness. A previously undescribed syndrome.
    Morris J; Ackerman B; Koblenzer PJ
    Arch Dermatol; 1969 Dec; 100(6):692-8. PubMed ID: 5365216
    [No Abstract]   [Full Text] [Related]  

  • 38. [Rubinstein-Taybi syndrome in a 2-year-old boy].
    Bartkowiak K; Olejniczakowa T
    Pediatr Pol; 1968 May; 43(5):637-40. PubMed ID: 5669065
    [No Abstract]   [Full Text] [Related]  

  • 39. [Idiopathic infantile hypercalcemia and Williams syndrome].
    Knudtzon J; Aarskog D
    Tidsskr Nor Laegeforen; 1986 Jun; 106(17-18):1488-91. PubMed ID: 3764822
    [No Abstract]   [Full Text] [Related]  

  • 40. Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.
    Zampino G; Mastroiacovo P; Ricci R; Zollino M; Segni G; Martini-Neri ME; Neri G
    Am J Med Genet; 1993 Aug; 47(2):176-83. PubMed ID: 8213903
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.