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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

124 related items for PubMed ID: 6660805

  • 1. [A complex malformation syndrome with brachymesomelia].
    Le Marec B, Bracq H, Picaud JC, Roussey M, Carsin M.
    Ann Pediatr (Paris); 1983 Nov; 30(9):721-4. PubMed ID: 6660805
    [No Abstract] [Full Text] [Related]

  • 2. Brachymesomelia-renal syndrome.
    Langer LO, Nishino R, Yamaguchi A, Ito Y, Ueke T, Togari H, Kato T, Opitz JM, Gilbert EF.
    Am J Med Genet; 1983 May; 15(1):57-65. PubMed ID: 6859124
    [Abstract] [Full Text] [Related]

  • 3. [The Silver-Russell syndrome].
    Bene M, Moga L.
    Rev Pediatr Obstet Ginecol Pediatr; 1980 May; 29(3):255-63. PubMed ID: 6781034
    [No Abstract] [Full Text] [Related]

  • 4. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.
    Goddeeris P, Fryns JP, van den Berghe H.
    J Genet Hum; 1980 Mar; 28(1):57-60. PubMed ID: 7400786
    [Abstract] [Full Text] [Related]

  • 5. [Whistling face syndrome (Burian)].
    Rickhey B.
    Z Orthop Ihre Grenzgeb; 1971 Jul; 109(3):532-4. PubMed ID: 4254815
    [No Abstract] [Full Text] [Related]

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

  • 7. Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clue.
    Hersh JH, Weisskopf B, DeCoster C.
    Am J Med Genet; 1984 Jun; 18(2):195-9. PubMed ID: 6465196
    [Abstract] [Full Text] [Related]

  • 8. O--short stature with abnormalities of the cranium and limbs.
    Jorgenson RJ.
    Birth Defects Orig Artic Ser; 1974 Jun; 10(5):249-51. PubMed ID: 4469995
    [No Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. [Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects].
    Joannard A, Bost M, Pont J, Dieterlen M, Frappat P, Beaudoing A.
    Pediatrie; 1974 Dec 31; 29(8):825-41. PubMed ID: 4218311
    [No Abstract] [Full Text] [Related]

  • 11. [Multiple malformation in a subject with D-D translocation].
    Boncompagni P.
    Minerva Pediatr; 1967 Nov 24; 19(47):2107-13. PubMed ID: 5606106
    [No Abstract] [Full Text] [Related]

  • 12. [Malformative syndrome caused by amniotic bands].
    Fabris C, Prandi GM, Martano C, Mostert M.
    Minerva Pediatr; 1981 Jan 31; 33(2):91-4. PubMed ID: 7242483
    [No Abstract] [Full Text] [Related]

  • 13. ["V.A.C.T.E.R.L.": a new complex of congenital multiple abnormalities as a possible consequence of the teratogenic action of exogenous hormones taken during pregnancy].
    Buffoni L, Tarateta A, Pecorari D.
    Minerva Ginecol; 1976 May 31; 28(5):382-91. PubMed ID: 1018820
    [No Abstract] [Full Text] [Related]

  • 14. A suspected case of Abruzzo-Erickson syndrome.
    Kidner G, Taylor J, Patton MA, Taylor N.
    Cleft Palate Craniofac J; 2004 Sep 31; 41(5):565-7. PubMed ID: 15352866
    [Abstract] [Full Text] [Related]

  • 15. Epidemiology of limb-body wall complex in Japan.
    Kurosawa K, Imaizumi K, Masuno M, Kuroki Y.
    Am J Med Genet; 1994 Jun 01; 51(2):143-6. PubMed ID: 8092190
    [Abstract] [Full Text] [Related]

  • 16. New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay.
    Bagatelle R, Cassidy SB.
    Am J Med Genet; 1995 Jan 30; 55(3):367-71. PubMed ID: 7537019
    [Abstract] [Full Text] [Related]

  • 17. Congenital malformations of the hand and forearm in children: what radiologists should know.
    Aucourt J, Budzik JF, Manouvrier-Hanu S, Mézel A, Cotten A, Boutry N.
    Semin Musculoskelet Radiol; 2012 Apr 30; 16(2):146-58. PubMed ID: 22648430
    [Abstract] [Full Text] [Related]

  • 18. Craniofacial, limb, and abdominal anomalies in a distinct syndrome: relation to the spectrum of Pfeiffer syndrome type 3.
    Barone CM, Marion R, Shanske A, Argamaso RV, Shprintzen RJ.
    Am J Med Genet; 1993 Mar 15; 45(6):745-50. PubMed ID: 8456855
    [Abstract] [Full Text] [Related]

  • 19. [Ultrasonographic diagnosis of a combined malformation syndrome - hydrocephalus - evisceration and dysplasia of the extremities (author's transl)].
    Schmidt W, Heberling D, Boos R, Heinrich D.
    Z Geburtshilfe Perinatol; 1981 Jun 15; 185(3):183-6. PubMed ID: 7196655
    [Abstract] [Full Text] [Related]

  • 20. [Skeletal changes in a case of unusual chromosome aberration. (Patient with chromosome complex 48, XXXX-49, XXXXX: comparison with the syndrome 49,XXXXY].
    Dallapiccola B, Pistocchi GF.
    Radiol Med; 1968 Aug 15; 54(8):737-50. PubMed ID: 5190487
    [No Abstract] [Full Text] [Related]

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