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 *

136 related articles for article (PubMed ID: 847850)

  • 1. [49,XXXXX syndrome: apropos of a further case].
    Tumba A; Fryns JP; van OOTEGHEM G; van den Berghe H
    Union Med Can; 1977 Feb; 106(2):226-30. PubMed ID: 847850
    [No Abstract]   [Full Text] [Related]  

  • 2. [Trial classification of D group chromosome long arm deletions. Apropos of a 15q- case].
    Laurent C; Noel B; David M
    Ann Genet; 1971 Mar; 14(1):33-40. PubMed ID: 5314292
    [No Abstract]   [Full Text] [Related]  

  • 3. Costello syndrome.
    Der Kaloustian VM; Moroz B; McIntosh N; Watters AK; Blaichman S
    Am J Med Genet; 1991 Oct; 41(1):69-73. PubMed ID: 1951465
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The Freeman-Sheldon Syndrome].
    Aldinger G; Eulert J
    Z Orthop Ihre Grenzgeb; 1983; 121(5):630-3. PubMed ID: 6649811
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Costello syndrome and facio-cutaneous-skeletal syndrome.
    Philip N; Mancini J
    Am J Med Genet; 1993 Aug; 47(2):174-5. PubMed ID: 8213902
    [No Abstract]   [Full Text] [Related]  

  • 6. Marfanoid features and craniosynostosis: report of one case and review.
    Lacombe D; Battin J
    Clin Dysmorphol; 1993 Jul; 2(3):220-4. PubMed ID: 8287183
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings.
    Neu RL; Kajii T; Gardner LI; Nagyfy SF
    Pediatrics; 1971 Mar; 47(3):610-2. PubMed ID: 5547878
    [No Abstract]   [Full Text] [Related]  

  • 8. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG; Zackowski JL; Storto PD; Newlin A
    Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG; McConnachie P; Hadro TA
    Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brief clinical report: two children with de novo del(9p).
    Young RS; Bader P; Palmer CG; Kaler SG; Hodes ME
    Am J Med Genet; 1983 Apr; 14(4):751-7. PubMed ID: 6846405
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. Smith-Lemli-Opitz syndrome: report of a new case and review of the literature.
    Srsen S
    Acta Paediatr Acad Sci Hung; 1972; 13(4):301-8. PubMed ID: 4664661
    [No Abstract]   [Full Text] [Related]  

  • 13. [The Rubenstein-Taybi syndrome. Apropos of a case].
    Jéliu G; Saint-Rome G
    Union Med Can; 1967 Jan; 96(1):22-9. PubMed ID: 6036674
    [No Abstract]   [Full Text] [Related]  

  • 14. [Associated malformations of the head and extremities].
    Tridon P
    J Genet Hum; 1974 Dec; 22(4):365-80. PubMed ID: 4282383
    [No Abstract]   [Full Text] [Related]  

  • 15. 49,XXXXX syndrome.
    Fragoso R; Hernandez A; Plascencia ML; Nazara Z; Martinez y Martinez R; Cantu JM
    Ann Genet; 1982; 25(3):145-8. PubMed ID: 6982661
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The dermatoglyphics of the 18q- syndrome.
    Mavalwala J; Wilson MG; Parker CE
    Am J Phys Anthropol; 1970 May; 32(3):443-9. PubMed ID: 5419379
    [No Abstract]   [Full Text] [Related]  

  • 17. Sandrow syndrome of mirror hands and feet and facial abnormalities.
    Kogekar N; Teebi AS; Vockley J
    Am J Med Genet; 1993 Apr; 46(2):126-8. PubMed ID: 8387243
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant.
    Papadia F; Zimbalatti F; La Rosa CG
    Am J Med Genet; 1984 Apr; 17(4):841-7. PubMed ID: 6720749
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [An uncommon malformation-retardation syndrome with "sheep-like face" and associated with autosomal structural aberration (author's transl)].
    Wiedemann HR; Tolksdorf M
    Klin Padiatr; 1973 Sep; 185(5):346-51. PubMed ID: 4797673
    [No Abstract]   [Full Text] [Related]  

  • 20. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML
    Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.