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Journal Abstract Search

372 related items for PubMed ID: 2301471

  • 1. Autosomal recessive Robinow syndrome.
    Teebi AS.
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
    [Abstract] [Full Text] [Related]

  • 2. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
    Saal HM, Greenstein RM, Weinbaum PJ, Poole AE.
    Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?
    Farag TI, Teebi AS.
    Am J Med Genet; 1990 Apr; 35(4):516-8. PubMed ID: 2333881
    [Abstract] [Full Text] [Related]

  • 4. [Robinow's syndrome associated with deafness].
    Samoud A, Menif K, Boulaares M, Ben Dridi MF.
    Arch Fr Pediatr; 1993 Dec; 50(10):897-9. PubMed ID: 8053771
    [Abstract] [Full Text] [Related]

  • 5. [Variable expression of an autosomal dominant syndrome: (BBB syndrome or G syndrome)].
    Le Merrer M, Verloes A, Narcy P, Briard ML.
    J Genet Hum; 1988 Jun; 36(3):257-64. PubMed ID: 3411306
    [Abstract] [Full Text] [Related]

  • 6. Frontofacionasal dysplasia: evidence for autosomal recessive inheritance.
    Gollop TR, Kiota MM, Martins RM, Lucchesi EA, Alvarenga Filho E.
    Am J Med Genet; 1984 Oct; 19(2):301-5. PubMed ID: 6439039
    [Abstract] [Full Text] [Related]

  • 7. Aarskog syndrome: report of a family with review and discussion of nosology.
    Teebi AS, Rucquoi JK, Meyn MS.
    Am J Med Genet; 1993 Jun 15; 46(5):501-9. PubMed ID: 8322809
    [Abstract] [Full Text] [Related]

  • 8. Geleophysic dysplasia.
    Wraith JE, Bankier A, Chow CW, Danks DM, Sardharwalla IB.
    Am J Med Genet; 1990 Feb 15; 35(2):153-6. PubMed ID: 2090119
    [Abstract] [Full Text] [Related]

  • 9. Autosomal recessive Silver-Russell syndrome.
    Teebi AS.
    Clin Dysmorphol; 1992 Jul 15; 1(3):151-6. PubMed ID: 1285272
    [Abstract] [Full Text] [Related]

  • 10. Chondrodystrophic myotonia (Schwartz-Jampel syndrome): report of a new case and follow-up of patients initially reported in 1969.
    Edwards WC, Root AW.
    Am J Med Genet; 1982 Sep 15; 13(1):51-6. PubMed ID: 7137221
    [Abstract] [Full Text] [Related]

  • 11.
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  • 12. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.
    Am J Med Genet; 1992 Jan 01; 42(1):112-6. PubMed ID: 1308349
    [Abstract] [Full Text] [Related]

  • 13. Urofacial (ochoa) syndrome.
    Ochoa B, Gorlin RJ.
    Am J Med Genet; 1987 Jul 01; 27(3):661-7. PubMed ID: 3631137
    [Abstract] [Full Text] [Related]

  • 14. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, Tillemans AA.
    Am J Med Genet; 1989 Dec 01; 34(4):593-600. PubMed ID: 2624276
    [Abstract] [Full Text] [Related]

  • 15. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Miny P, Lenz W.
    Am J Med Genet; 1985 Jun 01; 21(2):317-24. PubMed ID: 4014313
    [Abstract] [Full Text] [Related]

  • 16. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA, García-Cruz D, García-Cruz O, Sánchez-Corona J.
    Am J Med Genet; 1995 Feb 13; 55(4):420-2. PubMed ID: 7762580
    [Abstract] [Full Text] [Related]

  • 17. Robinow Syndrome: a case report.
    Gulcan H, Akinci A, Aktar A.
    Genet Couns; 2005 Feb 13; 16(3):297-300. PubMed ID: 16259327
    [Abstract] [Full Text] [Related]

  • 18. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
    Chudley AE, Rozdilsky B, Houston CS, Becker LE, Knoll JH.
    Am J Med Genet; 1985 Jan 13; 20(1):145-58. PubMed ID: 3970066
    [Abstract] [Full Text] [Related]

  • 19. A new short rib syndrome: report of two cases.
    Beemer FA, Langer LO, Klep-de Pater JM, Hemmes AM, Bylsma JB, Pauli RM, Myers TL, Haws CC.
    Am J Med Genet; 1983 Jan 13; 14(1):115-23. PubMed ID: 6829599
    [Abstract] [Full Text] [Related]

  • 20. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
    Pena SD, Shokeir MH.
    Birth Defects Orig Artic Ser; 1976 Jan 13; 12(5):201-8. PubMed ID: 953225
    [No Abstract] [Full Text] [Related]

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