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Journal Abstract Search

190 related items for PubMed ID: 14213965

  • 1. 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]

  • 2. A CASE OF XXXXY SEX CHROMOSOME ANOMALY WITH AUTORADIOGRAPHIC STUDIES.
    ATKINS L, BOEOEK JA, GUSTAVSON KH, HANSSON O, HJELM M.
    Cytogenetics; 1963 Dec; 2():208-31. PubMed ID: 14104167
    [No Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [THE POTTER SYNDROME (BILATERAL RENAL AGENESIS, FACIAL CHANGES AND OLIGOHYDRAMNIOS). STUDY OF A CASE].
    RASORE-QUARTINO A, DEPAULINI GC.
    Pathologica; 1963 Sep; 55():459-62. PubMed ID: 14153633
    [No Abstract] [Full Text] [Related]

  • 5. [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 18; 257():3098-102. PubMed ID: 14095841
    [No Abstract] [Full Text] [Related]

  • 6. [ON CONGENITAL FACIAL PARALYSIS].
    BALDUS S.
    Monatsschr Ohrenheilkd Laryngorhinol; 1964 Jan 18; 98():25-30. PubMed ID: 14182791
    [No Abstract] [Full Text] [Related]

  • 7. OCULO-AURICULO-VERTEBRAL SYNDROME. (GOLDENHAR'S SYNDROME).
    SMITHELLS RW.
    Dev Med Child Neurol; 1964 Aug 18; 6():406-7. PubMed ID: 14210665
    [No Abstract] [Full Text] [Related]

  • 8. [The ear in Crouzon's and Apert's craniofacial abnormalities].
    Terrahe K.
    Z Laryngol Rhinol Otol; 1971 Nov 18; 50(11):794-802. PubMed ID: 5131409
    [No Abstract] [Full Text] [Related]

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  • 11. CONGENITAL FOCAL DERMAL HYPOPLASIA.
    MARTIN-SCOTT I.
    Br J Dermatol; 1965 Jan 18; 77():60-2. PubMed ID: 14252686
    [No Abstract] [Full Text] [Related]

  • 12. [ATYPICAL FORM OF THE PIERRE ROBIN SYNDROME. PRESENTATION OF 2 CASES].
    PERALTASERRANO A.
    Rev Clin Esp; 1964 Apr 15; 93():47-50. PubMed ID: 14150288
    [No Abstract] [Full Text] [Related]

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  • 18. [SYMPOSIUM ON THE GENERAL CARE OF THE NORMAL AND PATHOLOGICAL NEWBORN. II. PATHOLOGY OF THE NEWBORN. B. CONGENITAL MALFORMATIONS: DIAGNOSIS AND MANAGEMENT IN THE NEONATAL PERIOD].
    DE PENNA HA, CURTI P, MANISSADJIAN A, BARBIERI D.
    Rev Paul Med; 1964 Jun 15; 64():321-407. PubMed ID: 14171499
    [No Abstract] [Full Text] [Related]

  • 19. [THE MALFORMATIVE SYNDROME OF CHROMOSOME 18 TRISOMY].
    NIGRO N, FRANCESCHINI P, VOLANTE G.
    Minerva Pediatr; 1964 Apr 21; 16():471-80. PubMed ID: 14158345
    [No Abstract] [Full Text] [Related]

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