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Journal Abstract Search

322 related items for PubMed ID: 4398858

  • 21. [Pulmonary artery stenosis, Pigmentary cutaneous spots and bone abnormalities. 4 cases].
    Pernot C, Deschamps JP, Didier F.
    Arch Fr Pediatr; 1971; 28(6):593-603. PubMed ID: 5000449
    [No Abstract] [Full Text] [Related]

  • 22. Association of hypertelorism and hypospadias--the BBB-syndrome.
    Michaelis E, Mortier W.
    Helv Paediatr Acta; 1972 Dec; 27(6):575-81. PubMed ID: 4405408
    [No Abstract] [Full Text] [Related]

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  • 26. [Systematized lentiginosis with congenital deafness and discrete status dysraphicus].
    Hornstein OP, Weidner F.
    Dermatologica; 1971 Dec; 143(2):79-83. PubMed ID: 4333206
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  • 28. [Multiple pterygium syndrome in children. 7 cases].
    Fenoll B, Rigault P, Maroteaux P, Padovani JP, Guyonvarch G, Durand Y.
    Rev Chir Orthop Reparatrice Appar Mot; 1990 Dec; 76(2):102-11. PubMed ID: 2142314
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  • 29. LEOPARD syndrome: what are café noir spots?
    Rodríguez-Bujaldón A, Vazquez-Bayo C, Jimenez-Puya R, Galan-Gutierrez M, Moreno-Gimenez J, Rodriguez-Garcia A, Tercedor J, Velez-Garcia A.
    Pediatr Dermatol; 2008 Dec; 25(4):444-8. PubMed ID: 18789084
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  • 30. The Noonan syndrome--a review of the clinical and genetic features of 27 cases.
    Collins E, Turner G.
    J Pediatr; 1973 Dec; 83(6):941-50. PubMed ID: 4148394
    [No Abstract] [Full Text] [Related]

  • 31. [Recommendations for the evaluation and interpretation of electrocardiograms in childhood--Clinical electrocardiography. 5. ECG after stress on the right ventricle].
    Bartel J, Mücke D.
    Z Arztl Fortbild (Jena); 1977 Jun 15; 71(12):586-92. PubMed ID: 143805
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  • 33. Hypertelorism and Waardenburg's syndrome.
    Ulivelli A, Silenzi M.
    Helv Paediatr Acta; 1969 Feb 15; 24(1):123-6. PubMed ID: 5801819
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  • 36. Acrofacial dysostosis with growth and mental retardation in three males, one with simultaneous Hermansky-Pudlak syndrome.
    Kelly TE, Cooke RJ, Kester RW.
    Birth Defects Orig Artic Ser; 1977 Feb 15; 13(3B):45-52. PubMed ID: 890099
    [No Abstract] [Full Text] [Related]

  • 37. [Ring chromosome 18. 18p-/18q- -deletion-syndrome].
    Kunze J, Stephan E, Tolksdorf M.
    Humangenetik; 1972 Feb 15; 15(4):289-318. PubMed ID: 4565746
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  • 38. Pigmentary anomalies in the multiple lentigines syndrome: Is it distinct from LEOPARD syndrome?
    Arnsmeier SL, Paller AS.
    Pediatr Dermatol; 1996 Feb 15; 13(2):100-4. PubMed ID: 9122064
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  • 39. A study of a family with leopard syndrome.
    Loyd DW, Tsuang MT, Benge JW.
    J Clin Psychiatry; 1982 Mar 15; 43(3):113-6. PubMed ID: 7061405
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