These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

112 related items for PubMed ID: 3220568

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism, and mental retardation.
    Imaizumi K, Kuroki Y.
    Am J Med Genet; 1991 Nov 01; 41(2):162-3. PubMed ID: 1785626
    [No Abstract] [Full Text] [Related]

  • 23. [18p-syndrome].
    Ieshima A.
    Ryoikibetsu Shokogun Shirizu; 2000 Nov 01; (30 Pt 5):335-6. PubMed ID: 11057251
    [No Abstract] [Full Text] [Related]

  • 24. Robinow syndrome in two siblings from consanguineous parents.
    Schorderet DF, Dahoun S, Defrance I, Nusslé D, Morris MA.
    Eur J Pediatr; 1992 Aug 01; 151(8):586-9. PubMed ID: 1505578
    [Abstract] [Full Text] [Related]

  • 25. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant.
    Papadia F, Zimbalatti F, La Rosa CG.
    Am J Med Genet; 1984 Apr 01; 17(4):841-7. PubMed ID: 6720749
    [Abstract] [Full Text] [Related]

  • 26. Robinow syndrome.
    Hosalkar HS, Gerardi J, Shaw BA.
    J Postgrad Med; 2002 Apr 01; 48(1):50-1. PubMed ID: 12082331
    [No Abstract] [Full Text] [Related]

  • 27. A case of Aarskog syndrome with a review of Japanese literature.
    Aihara K, Nishi Y, Usui T.
    Hiroshima J Med Sci; 1982 Jun 01; 31(2):87-90. PubMed ID: 7129954
    [No Abstract] [Full Text] [Related]

  • 28. [Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome].
    Franceschini P, Franceschini D.
    Minerva Pediatr; 1994 Dec 01; 46(12):579-80. PubMed ID: 7731422
    [No Abstract] [Full Text] [Related]

  • 29. Robinow Syndrome: a case report.
    Gulcan H, Akinci A, Aktar A.
    Genet Couns; 2005 Dec 01; 16(3):297-300. PubMed ID: 16259327
    [Abstract] [Full Text] [Related]

  • 30. Bartsocas-Papas syndrome in a Pakistani family from Kuwait.
    Al-Sawan RM, Soni AL, Al-Nakkas EM, Gang RK.
    Indian Pediatr; 2004 Jul 01; 41(7):725-7. PubMed ID: 15297688
    [Abstract] [Full Text] [Related]

  • 31. [Robinow syndrome (fetal-face dwarfism). Presentation of a case and review of the literature].
    Rodríguez Costa T, García De León R, Casas Fernández C, Puche Mira A, Pérez Bryan J.
    An Esp Pediatr; 1984 Jan 01; 20(1):55-61. PubMed ID: 6703533
    [Abstract] [Full Text] [Related]

  • 32. Midtrimester prenatal diagnosis of short-limb dwarfism (Saldino-Noonan syndrome).
    Johnson VP, Petersen LP, Holzwarth DR, Messner FD.
    Birth Defects Orig Artic Ser; 1982 Jan 01; 18(3 Pt A):133-41. PubMed ID: 7126786
    [No Abstract] [Full Text] [Related]

  • 33. [Robinow's syndrome. Apropos of a case with thrombopenia].
    Khayat D, Schaison G, Frija J, Szpirglas H.
    Arch Fr Pediatr; 1983 Apr 01; 40(4):327-30. PubMed ID: 6683959
    [Abstract] [Full Text] [Related]

  • 34. A novel variant in WNT5A responsible for Robinow syndrome in a male fetus with limb shortening and agenesis of the penis.
    Zhu H, Chen Y, Niu Y, Zhang Y, Chen L.
    Clin Dysmorphol; 2022 Apr 01; 31(2):71-73. PubMed ID: 34750320
    [No Abstract] [Full Text] [Related]

  • 35. [The "Charlie M." syndrome: a new clinical entity? Description of a case].
    Bonioli E, Sbolgi P, Bernaola E, Pacciani G, Cottafava F.
    Minerva Pediatr; 1980 May 31; 32(10):699-702. PubMed ID: 6779104
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Popliteal pterygium syndrome.
    Herold HZ, Shmueli G, Baruchin AM.
    Clin Orthop Relat Res; 1986 Aug 31; (209):194-7. PubMed ID: 3731594
    [Abstract] [Full Text] [Related]

  • 38. [Aarskog syndrome (author's transl)].
    Kunze J, Spranger J.
    Klin Padiatr; 1973 Nov 31; 185(6):490-4. PubMed ID: 4798676
    [No Abstract] [Full Text] [Related]

  • 39. [Robinow syndrome].
    Matsumoto T, Kondoh T.
    Ryoikibetsu Shokogun Shirizu; 2001 Nov 31; (34 Pt 2):591-2. PubMed ID: 11528913
    [No Abstract] [Full Text] [Related]

  • 40. Congenital heart defects in Aarskog syndrome.
    Fernandez I, Tsukahara M, Mito H, Yoshii H, Uchida M, Matsuo K, Kajii T.
    Am J Med Genet; 1994 May 01; 50(4):318-22. PubMed ID: 8209909
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 6.