BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 14210861)

  • 1. HOLOPROSENCEPHALY: A CASE REPORT WITH NO EXTRACRANIAL ABNORMALITIES AND NORMAL CHROMOSOME COUNT AND KARYOTYPE.
    BISHOP K; CONNOLLY JM; CARTER CH; CARPENTER DG
    J Pediatr; 1964 Sep; 65():406-14. PubMed ID: 14210861
    [No Abstract]   [Full Text] [Related]  

  • 2. FAMILIAL CHROMOSOME-2, 3 TRANSLOCATION ASCERTAINED THROUGH AN INFANT WITH MULTIPLE MALFORMATIONS.
    LEE CS; BOWEN P; ROSENBLUM H; LINSAO L
    N Engl J Med; 1964 Jul; 271():12-6. PubMed ID: 14148222
    [No Abstract]   [Full Text] [Related]  

  • 3. FAMILIAL ALOBAR HOLOPROSENCEPHALY (ARHINENCEPHALY) WITH MEDIAN CLEFT LIP AND PALATE. REPORT OF PATIENT WITH 46 CHROMOSOMES.
    DEMYER W; ZEMAN W; PALMER CD
    Neurology; 1963 Nov; 13():913-8. PubMed ID: 14079950
    [No Abstract]   [Full Text] [Related]  

  • 4. [ON 4 CASES OF ARHINENCEPHALIA. (CLINICAL STUDY)].
    MORETTI M; FAIENXA C
    Lattante; 1964 Jun; 35():297-304. PubMed ID: 14194466
    [No Abstract]   [Full Text] [Related]  

  • 5. THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY).
    DEMYER W; ZEMAN W; PALMER CG
    Pediatrics; 1964 Aug; 34():256-63. PubMed ID: 14211086
    [No Abstract]   [Full Text] [Related]  

  • 6. ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS.
    JACOBSON TS; TISCHLER B; MILLER JR
    Ann Hum Genet; 1964 Sep; 28():21-6. PubMed ID: 14204849
    [No Abstract]   [Full Text] [Related]  

  • 7. CONGENITAL MALFORMATIONS. CLINICAL AND COMMUNITY CONSIDERATIONS.
    INGALLS TH; KLINGBERG MA
    Am J Med Sci; 1965 Mar; 249():316-44. PubMed ID: 14273322
    [No Abstract]   [Full Text] [Related]  

  • 8. FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.
    UCHIDA IA; MCRAE KN; RAY M
    Am J Hum Genet; 1965 Sep; 17(5):410-9. PubMed ID: 14334740
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 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. Aicardi syndrome with holoprosencephaly and cleft lip and palate.
    Sato N; Matsuishi T; Utsunomiya H; Yamashita Y; Horikoshi T; Okudera T; Hashimoto T
    Pediatr Neurol; 1987; 3(2):114-6. PubMed ID: 3508052
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Otorhinolaryngologic manifestations of Hartsfield syndrome: Case series and review of literature.
    Oliver JD; Menapace DC; Cofer SA
    Int J Pediatr Otorhinolaryngol; 2017 Jul; 98():4-8. PubMed ID: 28583501
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [ATYPICAL FORM OF THE PIERRE ROBIN SYNDROME. PRESENTATION OF 2 CASES].
    PERALTASERRANO A
    Rev Clin Esp; 1964 Apr; 93():47-50. PubMed ID: 14150288
    [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. Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence.
    Yu FC; Gutman LT; Huang SW; Fresh JW; Emanuel I
    J Med Genet; 1970 Jun; 7(2):132-7. PubMed ID: 5519598
    [No Abstract]   [Full Text] [Related]  

  • 16. MALFORMATIONS OF THE EAR.
    WOLFF D
    Arch Otolaryngol; 1964 Mar; 79():288-301. PubMed ID: 14090429
    [No Abstract]   [Full Text] [Related]  

  • 17. CRANIOTELENCEPHALIC DYSPLASIA. AN UNUSUAL EXAMPLE OF DYSPLASIA OF FRONTAL BONE.
    JABBOUR JT; TAYBI H
    Am J Dis Child; 1964 Dec; 108():627-32. PubMed ID: 14213965
    [No Abstract]   [Full Text] [Related]  

  • 18. Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21).
    Witters I; Balikova I; Cannie M; Devriendt K; De Catte L; Fryns JP
    Genet Couns; 2008; 19(4):443-6. PubMed ID: 19239091
    [No Abstract]   [Full Text] [Related]  

  • 19. [CHROMOSOME ABNORMALITIES AND HUMAN DISEASES. CONTRIBUTION TO THE ANATOMICAL STUDY OF TRISOMY 13].
    LAFOURCADE J; BOCQUET L; CRUVEILLER J; SARAUX H; BERGER R; LEJEUNE J; HUETDEBAROCHEZ Y; TURPIN R
    Bull Mem Soc Med Hop Paris; 1964 Mar 6-13; 115():383-99. PubMed ID: 14156094
    [No Abstract]   [Full Text] [Related]  

  • 20. THE INNER EAR IN GENETICALLY DETERMINED DEAFNESS. REPORT AND ANALYSIS OF 2 NEW CASES.
    ALTMANN F
    Acta Otolaryngol Suppl; 1964; 175():SUPPL187:1-39. PubMed ID: 14115458
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.