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 *

320 related articles for article (PubMed ID: 14119520)

  • 1. A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.
    SMITH DW; LEMLI L; OPITZ JM
    J Pediatr; 1964 Feb; 64():210-7. PubMed ID: 14119520
    [No Abstract]   [Full Text] [Related]  

  • 2. A FAMILIAL SYNDROME OF FACIAL AND SKELETAL ANOMALIES ASSOCIATED WITH GENITAL ABNORMALITY IN THE MALE AND NORAML GENITALS IN THE FEMALE: ANOTHER CAUSE OF MALE PSEUDOHERMAPHRODITISM.
    PINSKY L; DIGEORGE AM
    J Pediatr; 1965 Jun; 66():1049-54. PubMed ID: 14288458
    [No Abstract]   [Full Text] [Related]  

  • 3. A CASE OF THE SMITH-LEMLI-OPITZ SYNDROME OF MULTIPLE CONGENITAL ANOMALIES IN ASSOCIATION WITH DYSPLASIA EPIPHYSIALIS PUNCTATA.
    GIBSON R
    Can Med Assoc J; 1965 Mar; 92(11):574-5. PubMed ID: 14303408
    [No Abstract]   [Full Text] [Related]  

  • 4. Smith-Lemli-Opitz syndrome: review and report of two affected siblings.
    Johnson VP
    Z Kinderheilkd; 1975; 119(4):221-34. PubMed ID: 166525
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 'IS THIS A SYNDROME?' NO. 1 OF A SERIES.
    SMITHELLS RW
    Dev Med Child Neurol; 1964 Dec; 6():606-9. PubMed ID: 14248479
    [No Abstract]   [Full Text] [Related]  

  • 6. BRACHYDACTYLY, PECULIAR FACIES AND MENTAL RETARDATION.
    COFFIN GS
    Am J Dis Child; 1964 Oct; 108():351-9. PubMed ID: 14186654
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. [LEPRECHAUNISM. (APROPOS OF A LITTLE KNOWN FORM OF FAMILIAL OLIGOPHRENIA)].
    BAMATTER F
    Rev Med Suisse Romande; 1964 Jun; 84():494-502. PubMed ID: 14187829
    [No Abstract]   [Full Text] [Related]  

  • 9. THE DE LANGE SYNDROME: REPORT OF THREE CASES.
    GIBSON R
    Can Med Assoc J; 1964 Sep; 91(12):643-6. PubMed ID: 14201252
    [TBL] [Abstract][Full Text] [Related]  

  • 10. THE "CAT CRY" SYNDROME.
    MACINTYRE MN; STAPLES WI; LAPOLLA J; HEMPEL JM
    Am J Dis Child; 1964 Nov; 108():538-42. PubMed ID: 14209690
    [No Abstract]   [Full Text] [Related]  

  • 11. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients.
    Guion-Almeida ML; Zechi-Ceide RM; Richieri-Costa A
    Am J Med Genet; 1999 Nov; 87(1):72-7. PubMed ID: 10528252
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progeroid syndrome with characteristic facial appearance and hand anomalies in father and son.
    Giannotti A; Digilio MC; Mingarelli R; Marino B; Dallapiccola B
    Am J Med Genet; 1997 Dec; 73(2):227-9. PubMed ID: 9409877
    [TBL] [Abstract][Full Text] [Related]  

  • 13. THE DE LANGE SYNDROME.
    HART ZH; JASLOW RI; GOMEZ MR
    Am J Dis Child; 1965 Apr; 109():325-32. PubMed ID: 14261013
    [No Abstract]   [Full Text] [Related]  

  • 14. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
    Dallaire L
    J Med Genet; 1969 Jun; 6(2):113-20. PubMed ID: 4389828
    [No Abstract]   [Full Text] [Related]  

  • 15. [4 CASES OF PERIPHERAL DYSOSTOSIS OCCURRING IN 1 FAMILY].
    BOREJKO M; DUCHOWSKA H
    Reumatologia; 1965; 3():69-74. PubMed ID: 14327368
    [No Abstract]   [Full Text] [Related]  

  • 16. A second patient with Tsukahara syndrome: type A1 brachydactyly, short stature, hearing loss, microcephaly, mental retardation and ptosis.
    Utine GE; Breckpot J; Thienpont B; Alanay Y; Aksoy C; Boduroğlu K; Devriendt K
    Am J Med Genet A; 2010 Apr; 152A(4):947-9. PubMed ID: 20358606
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features.
    Vinkler C; Leshinsky-Silver E; Michelson M; Haas D; Lerman-Sagie T; Lev D
    Eur J Med Genet; 2014; 57(6):288-92. PubMed ID: 24709618
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A syndrome with true anophthalmia, hand-foot defects and mental retardation.
    Pallotta R; Dallapiccola B
    Ophthalmic Paediatr Genet; 1984 Apr; 4(1):19-23. PubMed ID: 6544388
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TRISOMY-18 SYNDROME: CASE REPORT WITH CHROMOSOMAL ANALYSIS.
    GOLDSTONE RM; MOTSAY DS
    Guthrie Clin Bull; 1964 Jan; 33():108-16. PubMed ID: 14109161
    [No Abstract]   [Full Text] [Related]  

  • 20. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
    Bartsocas CS; Papas CV
    J Med Genet; 1972 Jun; 9(2):222-6. PubMed ID: 4339984
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.