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Journal Abstract Search

211 related items for PubMed ID: 14151466

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  • 3. A MOSAIC MONGOL WITH NORMAL LEUCOCYTE CHROMOSOMES.
    RIDLER MA, SHAPIRO A, DELHANTY JD, SMITH GF.
    Br J Psychiatry; 1965 Feb; 111():183-5. PubMed ID: 14270531
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  • 6. [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; 64():321-407. PubMed ID: 14171499
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  • 7. [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
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  • 8. CONGENITAL MALFORMATIONS. CLINICAL AND COMMUNITY CONSIDERATIONS.
    INGALLS TH, KLINGBERG MA.
    Am J Med Sci; 1965 Mar 15; 249():316-44. PubMed ID: 14273322
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  • 12. [Apropos of several congenital malformations observed in the Congo].
    BROWNE SG.
    Ann Soc Belg Med Trop (1920); 1962 Jun 30; 42():295-8. PubMed ID: 14016081
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  • 14. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E, Leze H, Katana A, Kolialexi A, Mavrou A, Kanavakis E, Kitsiou-Tzeli S.
    Genet Couns; 2009 Jun 30; 20(2):181-7. PubMed ID: 19650416
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  • 15. Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling.
    Patil SJ, Ponnala R, Shah S, Dalal A.
    Indian J Pediatr; 2012 Jun 30; 79(6):806-9. PubMed ID: 21975655
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  • 16. [RARE MALFORMATIONS OF THE FACE].
    MOYSON F, JEANTY M.
    Arch Fr Pediatr; 1964 Oct 30; 21():939-55. PubMed ID: 14195289
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  • 19. [THE POTTER SYNDROME (BILATERAL RENAL AGENESIS, FACIAL CHANGES AND OLIGOHYDRAMNIOS). STUDY OF A CASE].
    RASORE-QUARTINO A, DEPAULINI GC.
    Pathologica; 1963 Oct 30; 55():459-62. PubMed ID: 14153633
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