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 *

125 related articles for article (PubMed ID: 8296273)

  • 1. [Problems of small patient groups, illustrated by Williams syndrome].
    Heiberg A
    Tidsskr Nor Laegeforen; 1994 Jan; 114(1):14. PubMed ID: 8296273
    [No Abstract]   [Full Text] [Related]  

  • 2. [Williams' syndrome in 2 children].
    Krajewska-Walasek M
    Wiad Lek; 1983 Jan; 36(2):155-9. PubMed ID: 6858144
    [No Abstract]   [Full Text] [Related]  

  • 3. [The ups and downs of Williams-Beuren syndrome].
    Dupuis C; Delga JM; Delga I
    Arch Pediatr; 1994 Jul; 1(7):629-32. PubMed ID: 7987459
    [No Abstract]   [Full Text] [Related]  

  • 4. [Elfin face syndrome - an often missed diagnosis].
    Zetterqvist P; Klackenberg G; Billing L; Bjarke B; Josephsson E; Lundström NR
    Lakartidningen; 1982 Apr; 79(14):1363-6. PubMed ID: 7087611
    [No Abstract]   [Full Text] [Related]  

  • 5. [Williams-Beuren syndrome in Norway].
    Bjørnstad PG
    Tidsskr Nor Laegeforen; 1994 Jan; 114(1):25-8. PubMed ID: 8296277
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cognitive and neuropsychological profiles in malformation syndromes: a comparison between Down's syndrome and Williams' syndrome within a follow-up].
    Capozzi F; Levi G; Sogos C
    Pediatr Med Chir; 1993; 15 Suppl 1():29-33. PubMed ID: 8415192
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The Williams-Beuren syndrome in a boy with mosaic Klinefelter's syndrome].
    Bzdúch V; Lukácová M; Beránková M; Bircák J
    Cesk Pediatr; 1989 Oct; 44(10):622-3. PubMed ID: 2620359
    [No Abstract]   [Full Text] [Related]  

  • 8. The Williams syndrome: evidence for possible autosomal dominant inheritance.
    Sadler LS; Robinson LK; Verdaasdonk KR; Gingell R
    Am J Med Genet; 1993 Sep; 47(4):468-70. PubMed ID: 8256806
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Monozygotic twins with Williams-Beuren or 'elfen-face' syndrome].
    Oorthuys JW
    Tijdschr Kindergeneeskd; 1984 Oct; 52(5):197-200. PubMed ID: 6542697
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Radioulnar synostosis in Williams-Beuren syndrome: a component manifestation.
    Pankau R; Gosch A; Wessel A
    Am J Med Genet; 1993 Mar; 45(6):783. PubMed ID: 8456863
    [No Abstract]   [Full Text] [Related]  

  • 11. [The syndrome of supravalvular aortic stenosis, mental retardation and peculiar facies].
    Alsac J; Guay JM; Paquet E
    Arch Mal Coeur Vaiss; 1973 Jun; 66(6):765-73. PubMed ID: 4199790
    [No Abstract]   [Full Text] [Related]  

  • 12. 'Typus edinburgensis' explained.
    Laing IA; Lyall EG; Hendry LM; Ellis PM
    Pediatrics; 1991 Jul; 88(1):151-4. PubMed ID: 2057251
    [No Abstract]   [Full Text] [Related]  

  • 13. [Williams-Beuren facies with mental retardation and tetralogy of Fallot].
    Pernot C; Worms AM; Marçon F; Admant P
    Pediatrie; 1984; 39(1):53-8. PubMed ID: 6739228
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [The Williams and Beuren syndrome: aspects of the elfin facies].
    Bezzi TM; Bergamini M; Scorrano M; Pinca A
    Pediatria (Napoli); 1983; 91(2-3):281-6. PubMed ID: 6664736
    [No Abstract]   [Full Text] [Related]  

  • 15. Kabuki syndrome and diaphragmatic defect.
    Sethi SK; Faridi MM
    Indian Pediatr; 2006 Jun; 43(6):552-3. PubMed ID: 16820668
    [No Abstract]   [Full Text] [Related]  

  • 16. [Williams syndrome. Considerations on an unusual case].
    Alpigiani MG; Franzone G; Puleo MG; Carpi A; Iester A
    Pediatr Med Chir; 1994; 16(1):85-6. PubMed ID: 8029098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disabilities of genetic origin.
    Sterling HM
    Arch Phys Med Rehabil; 1970 May; 51(5):291-6 passim. PubMed ID: 4246188
    [No Abstract]   [Full Text] [Related]  

  • 18. Abnormal regulation of circulating 25-hydroxyvitamin D in the Williams syndrome.
    Taylor AB; Stern PH; Bell NH
    N Engl J Med; 1982 Apr; 306(16):972-5. PubMed ID: 6977721
    [No Abstract]   [Full Text] [Related]  

  • 19. Picture of the month: infantile hypercalcemia with mental retardation.
    Gellis SS; Feingold M
    Am J Dis Child; 1968 Apr; 115(4):471-2. PubMed ID: 5642350
    [No Abstract]   [Full Text] [Related]  

  • 20. Williams syndrome--the enigma continues.
    Lancet; 1988 Aug; 2(8609):490. PubMed ID: 2900409
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.