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Journal Abstract Search

347 related items for PubMed ID: 6720746

  • 21. Thin ribs, thin tubular bones, abnormal facies and intrauterine growth retardation: a lethal syndrome.
    Sharma BK, Kapoor R, Ramji S, Thirupuram S, Suri M.
    Br J Radiol; 1990 Aug; 63(752):654-6. PubMed ID: 2400886
    [No Abstract] [Full Text] [Related]

  • 22. Multiple pterygium syndrome.
    Chen H, Chang CH, Misra RP, Peters HA, Grijalva NS, Opitz JM.
    Am J Med Genet; 1980 Aug; 7(2):91-102. PubMed ID: 7468651
    [Abstract] [Full Text] [Related]

  • 23. Omodysplasia.
    Maroteaux P, Sauvegrain J, Chrispin A, Farriaux JP.
    Am J Med Genet; 1989 Mar; 32(3):371-5. PubMed ID: 2729357
    [Abstract] [Full Text] [Related]

  • 24. Fetal cystic hygroma in sibs: developmental analysis of coexistent cardiovascular malformations relevant to pathogenesis.
    Miyabara S, Suzumori K, Uemura Y, Tokunaga M.
    Birth Defects Orig Artic Ser; 1993 Mar; 29(1):303-15. PubMed ID: 8280883
    [No Abstract] [Full Text] [Related]

  • 25. [Echographic diagnosis of cystic hygroma. Apropos of a case].
    Nguyen Tan Lung R, Lalau P.
    J Gynecol Obstet Biol Reprod (Paris); 1987 Mar; 16(7):893-900. PubMed ID: 3327879
    [Abstract] [Full Text] [Related]

  • 26. Nuchal cystic hygroma associated with massive lymphangiomatosis of the upper extremity and myocardium in a stillborn fetus: a case report.
    Walker WP, Landas SK.
    Am J Cardiovasc Pathol; 1990 Mar; 3(4):341-6. PubMed ID: 2151786
    [Abstract] [Full Text] [Related]

  • 27. Heterogeneity in fetal akinesia deformation sequence (FADS): autopsy confirmation in three 20-21-week fetuses.
    Yfantis H, Nonaka D, Castellani R, Harman C, Sun CC.
    Prenat Diagn; 2002 Jan; 22(1):42-7. PubMed ID: 11810649
    [Abstract] [Full Text] [Related]

  • 28. Prenatal diagnosis of cystic hygroma and chorioangioma in the Wolf-Hirschhorn syndrome.
    Verloes A, Schaaps JP, Herens C, Soyeur D, Hustin J, Dodinval P.
    Prenat Diagn; 1991 Feb; 11(2):129-32. PubMed ID: 2062819
    [Abstract] [Full Text] [Related]

  • 29. Autoptic and echocardiographic findings in seven foetuses with congenital heart anomalies, lung lobation defects and normal visceroatrial arrangement.
    Angiero F, Fesslova V, Rizzuti T, Stefani M.
    Pathologica; 2011 Jun; 103(3):53-60. PubMed ID: 22007565
    [Abstract] [Full Text] [Related]

  • 30. Fryns syndrome in a girl born to consanguineous parents.
    Schwyzer U, Briner J, Schinzel A.
    Acta Paediatr Scand; 1987 Jan; 76(1):167-71. PubMed ID: 3564997
    [Abstract] [Full Text] [Related]

  • 31. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
    Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R.
    Am J Med Genet; 1995 Nov 20; 59(3):329-33. PubMed ID: 8599356
    [Abstract] [Full Text] [Related]

  • 32. Craniomicromelic syndrome: a newly recognized lethal condition with craniosynostosis, distinct facial anomalies, short limbs, and intrauterine growth retardation.
    Barr M, Heidelberger KP, Comstock CH.
    Am J Med Genet; 1995 Sep 25; 58(4):348-52. PubMed ID: 8533844
    [Abstract] [Full Text] [Related]

  • 33. Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardation.
    Cormier-Daire V, Chauvet ML, Lyonnet S, Briard ML, Munnich A, Le Merrer M.
    J Med Genet; 2000 Jul 25; 37(7):520-4. PubMed ID: 10882755
    [Abstract] [Full Text] [Related]

  • 34. Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome.
    García-Ortiz JE, Castañeda-Cisneros G, López-Cardona MG, Sánchez-Corona J, Patiño-García B, García-González CL, Nazará Z, Dávalos-Rodríguez N, Rodríguez LX, García-Cruz D.
    Am J Med Genet A; 2006 Jun 01; 140(11):1245-9. PubMed ID: 16688750
    [No Abstract] [Full Text] [Related]

  • 35. Skeletal deformities of acardius anceps: the gross and imaging features.
    Chen CP, Shih SL, Liu FF, Jan SW, Lin YN, Lan CC.
    Pediatr Radiol; 1997 Mar 01; 27(3):221-5. PubMed ID: 9126574
    [Abstract] [Full Text] [Related]

  • 36. Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndrome.
    García-Cruz D, Rivera H, Barajas LO, Jiménez-Sáinz M, Nazará Z, Sánchez-Corona J, Durón-Huerta H, García-Ochoa C, Cantú JM.
    Ann Genet; 1985 Mar 01; 28(4):231-4. PubMed ID: 3879435
    [Abstract] [Full Text] [Related]

  • 37. Sonographic features of lethal multiple pterygium syndrome at 14 weeks.
    Chen M, Chan GS, Lee CP, Tang MH.
    Prenat Diagn; 2005 Jun 01; 25(6):475-8. PubMed ID: 15966038
    [Abstract] [Full Text] [Related]

  • 38. Lymphatic abnormalities in fetuses with posterior cervical cystic hygroma.
    Chitayat D, Kalousek DK, Bamforth JS.
    Am J Med Genet; 1989 Jul 01; 33(3):352-6. PubMed ID: 2801770
    [Abstract] [Full Text] [Related]

  • 39. Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS).
    Barnicoat AJ, Seller MJ, Bennett CP.
    Clin Dysmorphol; 1994 Oct 01; 3(4):353-7. PubMed ID: 7894742
    [Abstract] [Full Text] [Related]

  • 40. Second female case of Myhre syndrome.
    Lopez-Cardona MG, Garcia-Cruz D, Garcia-Ortiz JE, Davalos NO, Feria-Velasco A, Rodriguez-Rojas LX, Garcia-Cruz MO, Figuera-Villanueva LE, Stephens A, Larios-Arceo F, Sanchez-Corona J.
    Clin Dysmorphol; 2004 Apr 01; 13(2):91-94. PubMed ID: 15057124
    [Abstract] [Full Text] [Related]

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