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 *

135 related articles for article (PubMed ID: 14288458)

  • 21. [CLINICAL AND RADIOLOGICAL CONTRIBUTION TO THE STUDY OF ANOMALIES OF BONE IN MENTAL DISEASES. DYSMORPHOSIS AND OLIGOPHRENIA].
    DIMIZIO V; BUONDONNO E
    Minerva Med; 1964 Feb; 55():375-6. PubMed ID: 14139674
    [No Abstract]   [Full Text] [Related]  

  • 22. CHONDRODYSTROPHIA CALCIFICANS CONGENITA; CHONDRODYSPLASIA EPIPHYSIALIS PUNCTATA, STIPPLED EPIPHYSES.
    MELNICK JC
    Am J Dis Child; 1965 Aug; 110():218-25. PubMed ID: 14320779
    [No Abstract]   [Full Text] [Related]  

  • 23. CONGENITAL ANHIDROTIC ECTODERMAL DYSPLASIA; REPORT OF TWO CASES.
    HARTWELL SW; PICKRELL K; QUINN G
    Clin Pediatr (Phila); 1965 Jul; 4():383-6. PubMed ID: 14314501
    [No Abstract]   [Full Text] [Related]  

  • 24. FAMILIAL MALE PSEUDOHERMAPHRODITISM.
    BOCZKOWSKI K; TETER J
    Acta Endocrinol (Copenh); 1965 Aug; 49():497-509. PubMed ID: 14329824
    [No Abstract]   [Full Text] [Related]  

  • 25. A mental retardation syndrome with peripheral dysostosis and pug nose.
    McKusick VA
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):249-50. PubMed ID: 5173379
    [No Abstract]   [Full Text] [Related]  

  • 26. THE MANAGEMENT OF DEFORMITIES AND INJURIES OF THE FACIAL SKELETON.
    SUGRUE D
    J Ir Med Assoc; 1964 Apr; 54():114-7. PubMed ID: 14136842
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. BROAD THUMBS AND TOES, AND UNUSUAL FACIAL FEATURES; A PROBABLE MENTAL RETARDATION SYNDROME.
    TAYBI H; RUBINSTEIN JH
    Am J Roentgenol Radium Ther Nucl Med; 1965 Feb; 93():362-6. PubMed ID: 14258284
    [No Abstract]   [Full Text] [Related]  

  • 29. Case 04-1994: a six-week-old infant with multiple congenital anomalies and an abnormal respiratory pattern.
    Hegenbarth MA; Hoffman JM
    Pediatr Emerg Care; 1994 Aug; 10(4):244-8. PubMed ID: 7937307
    [No Abstract]   [Full Text] [Related]  

  • 30. CONGENITAL LIPODYSTROPHIC DIABETES WITH ACANTHOSIS NIGRICANS: THE SEIP-LAWRENCE SYNDROME.
    REED WB; DEXTER R; CORLEY C; FISH C
    Arch Dermatol; 1965 Apr; 91():326-34. PubMed ID: 14275494
    [No Abstract]   [Full Text] [Related]  

  • 31. Median cleft face syndrome.
    Edwards WC; Askew W; Weisskopf B
    Am J Ophthalmol; 1971 Jul; 72(1):202-5. PubMed ID: 5571207
    [No Abstract]   [Full Text] [Related]  

  • 32. NONSPECIFIC PSEUDOHERMAPHRODITISM : REPORT OF TWO CASES WITH CYTOGENETIC INVESTIGATIONS.
    FERRIER P; WIDGREN S; FERRIER S
    Helv Paediatr Acta; 1964 Jun; 19():1-12. PubMed ID: 14189839
    [No Abstract]   [Full Text] [Related]  

  • 33. Microcephaly, unusual nose, cutaneous syndactyly, and mental retardation.
    Hennekam RCM; Schrander-Stumpel CTRM
    Clin Dysmorphol; 2010 Oct; 19(4):212-214. PubMed ID: 20531167
    [No Abstract]   [Full Text] [Related]  

  • 34. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
    Verloes A; Dodinval P; Beco L; Bonnivert J; Lambotte C
    Am J Med Genet; 1990 Sep; 37(1):119-23. PubMed ID: 2240028
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?
    Wolff G; Zimmermann E; Zimmerhackl B; Harnasch C; Jung C; Back E
    J Med Genet; 1994 Jan; 31(1):65-7. PubMed ID: 8151642
    [TBL] [Abstract][Full Text] [Related]  

  • 36. STUDIES OF A FAMILY WITH THE ORAL-FACIAL-DIGITAL SYNDROME.
    DOEGE TC; THULINE HC; PRIEST JH; NORBY DE; BRYANT JS
    N Engl J Med; 1964 Nov; 271():1073-8. PubMed ID: 14210999
    [No Abstract]   [Full Text] [Related]  

  • 37. [CONSIDERATIONS ON A CASE OF BILATERAL CHOANAL ATRESIA IN A NEWBORN INFANT].
    VELCOVICI D; MAIOREANU A; SEGAL M
    Pediatria (Bucur); 1965; 14():165-9. PubMed ID: 14325100
    [No Abstract]   [Full Text] [Related]  

  • 38. [FAMILIAL ECTRODACTYLIA OF THE HANDS AND FEET].
    TOS L; POLLONO F
    Minerva Ortop; 1965 Apr; 16():185-90. PubMed ID: 14342904
    [No Abstract]   [Full Text] [Related]  

  • 39. [THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME].
    COUTEAU-LAGARDE JM; COLLIER M
    J Genet Hum; 1963 Dec; 12():146-53. PubMed ID: 14136826
    [No Abstract]   [Full Text] [Related]  

  • 40. PROBOSCIS LATERALIS.
    RAO PB
    J Laryngol Otol; 1963 Dec; 77():1028-31. PubMed ID: 14100981
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.