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 *

138 related articles for article (PubMed ID: 5577740)

  • 1. [13 R syndrome. Dr-syndrome].
    Mikkelsen M; Niebuhr E
    Ugeskr Laeger; 1971 Apr; 133(16):759. PubMed ID: 5577740
    [No Abstract]   [Full Text] [Related]  

  • 2. [A single D chromosome in ring form in a 2-year-old girl with mental retardation].
    Morić-Petrović S; Garzicić B; Despotović M; Kalicanin P
    Srp Arh Celok Lek; 1970 Mar; 98(3):447-52. PubMed ID: 5205520
    [No Abstract]   [Full Text] [Related]  

  • 3. [Supernumerary metacentric small chromosome in a boy with mental retardation].
    Antich J; Sabater J
    Arch Neurobiol (Madr); 1971; 34(4):315-24. PubMed ID: 4999565
    [No Abstract]   [Full Text] [Related]  

  • 4. [Freeman-Sheldon syndrome. Three new observations].
    Pfeiffer RA; Ammermann M; Baisch C; Böllhoff G
    Z Kinderheilkd; 1972; 112(1):43-53. PubMed ID: 5019025
    [No Abstract]   [Full Text] [Related]  

  • 5. Association of hypertelorism and hypospadias--the BBB-syndrome.
    Michaelis E; Mortier W
    Helv Paediatr Acta; 1972 Dec; 27(6):575-81. PubMed ID: 4405408
    [No Abstract]   [Full Text] [Related]  

  • 6. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B; Rosenfeld R; Cadotte M
    Union Med Can; 1974 Aug; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract]   [Full Text] [Related]  

  • 7. [Crying cat syndrome discovered during a routine examination].
    Lafon R; Emberger JM; Pouget R; Chiariny JF
    Ann Med Psychol (Paris); 1972; 2(3):431-8. PubMed ID: 4675135
    [No Abstract]   [Full Text] [Related]  

  • 8. Ring chromosome 15 syndrome.
    Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
    Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
    [No Abstract]   [Full Text] [Related]  

  • 9. [Reno-facial dysplasia. Potter-I-syndrome].
    Niederalt G; Türk M; Fischer R
    Med Welt; 1971 May; 21():865-8. PubMed ID: 5577593
    [No Abstract]   [Full Text] [Related]  

  • 10. [The Coffin-Siris syndrome. A new syndrome of mental retardation, hypo-aplasia of the nails and terminal phalanges of the 5th fingers and toes].
    Mastroiacovo P; Salvaggio E; Parenti D
    Minerva Pediatr; 1977 Mar; 29(11):773-8. PubMed ID: 875947
    [No Abstract]   [Full Text] [Related]  

  • 11. The syndrome of the metacentric microchromosome.
    Abbo G; Zellweger H
    Helv Paediatr Acta; 1970 Jan; 25(1):83-94. PubMed ID: 4392428
    [No Abstract]   [Full Text] [Related]  

  • 12. [The r(15) syndrome (ring chromosome 15). Description of a case].
    Ferrante E; Boscherini B; Bruni L; Vignetti P; Finocchi G
    Minerva Pediatr; 1977 Nov; 29(36):2163-8. PubMed ID: 600224
    [No Abstract]   [Full Text] [Related]  

  • 13. [18p-Syndrome. Deletion of the short arm of chromosome 18].
    Jacobsen P
    Ugeskr Laeger; 1973 Jan; 135(1):17. PubMed ID: 4684842
    [No Abstract]   [Full Text] [Related]  

  • 14. [3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
    LEJEUNE J; LAFOURCADE J; BERGER R; VIALATTE J; BOESWILLWALD M; SERINGE P; TURPIN R
    C R Hebd Seances Acad Sci; 1963 Nov; 257():3098-102. PubMed ID: 14095841
    [No Abstract]   [Full Text] [Related]  

  • 15. [Two malformative syndromes possibly unifiable: Ullrich-Feichtiger and Smith-Lemli-Opitz syndromes. Case report].
    Lendvai D; Castello MA; Ballati G
    Minerva Pediatr; 1969 Jan; 21(2):56-61. PubMed ID: 4388355
    [No Abstract]   [Full Text] [Related]  

  • 16. Ocular hypertelorism and nasal agenesis (midface syndrome) with limb anomalies.
    Calli LJ
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):268. PubMed ID: 5173220
    [No Abstract]   [Full Text] [Related]  

  • 17. [49, XXXXX syndrome in a 5-year-old girl].
    Larget-Piet L; Rivron J; Baillif P; Dugay J; Emerit I; Larget-Piet A; Berthelot J
    Ann Genet; 1972 Jun; 15(2):115-9. PubMed ID: 4537723
    [No Abstract]   [Full Text] [Related]  

  • 18. Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome.
    Horn D; Witkowski R
    Genet Couns; 1993; 4(4):305-9. PubMed ID: 8110420
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Smith-Lemli-Opitz syndrome. Case report and differential diagnosis].
    Domenici R; Fiorini V; Giorgi F
    Minerva Pediatr; 1982 Sep; 34(17):709-14. PubMed ID: 6292682
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.