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Journal Abstract Search

134 related items for 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
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  • 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
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  • 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
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  • 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 19; 271():1073-8. PubMed ID: 14210999
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  • 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 Nov 19; 3(2):114-6. PubMed ID: 3508052
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  • 12. Otorhinolaryngologic manifestations of Hartsfield syndrome: Case series and review of literature.
    Oliver JD, Menapace DC, Cofer SA.
    Int J Pediatr Otorhinolaryngol; 2017 Jul 19; 98():4-8. PubMed ID: 28583501
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  • 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 18; 257():3098-102. PubMed ID: 14095841
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  • 16. MALFORMATIONS OF THE EAR.
    WOLFF D.
    Arch Otolaryngol; 1964 Mar 18; 79():288-301. PubMed ID: 14090429
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  • 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 Mar 18; 19(4):443-6. PubMed ID: 19239091
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  • 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; 2008 Mar 18; 115():383-99. PubMed ID: 14156094
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  • 20. THE INNER EAR IN GENETICALLY DETERMINED DEAFNESS. REPORT AND ANALYSIS OF 2 NEW CASES.
    ALTMANN F.
    Acta Otolaryngol Suppl; 1964 Mar 18; 175():SUPPL187:1-39. PubMed ID: 14115458
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