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Journal Abstract Search

246 related items for PubMed ID: 3400735

  • 1. Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome.
    Pfeiffer RA, Stöss H, Voight HJ, Wündisch GF.
    Am J Med Genet; 1988 Apr; 29(4):901-8. PubMed ID: 3400735
    [Abstract] [Full Text] [Related]

  • 2. Fuhrmann syndrome of right-angle bowed femora, absence of fibulae and digital anomalies: two further cases.
    Lipson AH, Kozlowski K, Barylak A, Marsden W.
    Am J Med Genet; 1991 Nov 01; 41(2):176-9. PubMed ID: 1785629
    [Abstract] [Full Text] [Related]

  • 3. Walker-Warburg syndrome with cleft lip and cleft palate in two sibs.
    Burton BK, Dillard RG, Weaver RG.
    Am J Med Genet; 1987 Jul 01; 27(3):537-41. PubMed ID: 3631127
    [Abstract] [Full Text] [Related]

  • 4. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug 01; 12(4):377-409. PubMed ID: 7124793
    [Abstract] [Full Text] [Related]

  • 5. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A, Colletto GM, Gollop TR, Masiero D.
    Am J Med Genet; 1985 Apr 01; 20(4):631-8. PubMed ID: 2986457
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 28(1):57-60. PubMed ID: 7400786
    [Abstract] [Full Text] [Related]

  • 7. [Genetic characteristics of the "EEC" syndrome (ectrodactyly, ectodermal dysplasis, cheilognathopalatoschisis)].
    Lur'e IV, Laziuk GI, Usova IuI.
    Genetika; 1976 Mar 01; 12(7):125-31. PubMed ID: 1001885
    [Abstract] [Full Text] [Related]

  • 8. Ulnar agenesis and endocardial fibroelastosis.
    Marles SL, Chudley AE.
    Am J Med Genet; 1990 Oct 01; 37(2):258-60. PubMed ID: 2248295
    [Abstract] [Full Text] [Related]

  • 9. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
    Hsia YE, Bratu M, Herbordt A.
    Pediatrics; 1971 Aug 01; 48(2):237-47. PubMed ID: 4997860
    [No Abstract] [Full Text] [Related]

  • 10. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes.
    Dincsoy MY, Salih MA, al-Jurayyan N, al Saadi M, Patel PJ.
    Am J Med Genet; 1995 Apr 10; 56(3):317-21. PubMed ID: 7778599
    [Abstract] [Full Text] [Related]

  • 11. Robin sequence and oligodactyly in mother and son.
    Robinow M, Johnson GF, Apesos J.
    Am J Med Genet; 1986 Oct 10; 25(2):293-7. PubMed ID: 3777025
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis).
    Elejalde BR, de Elejalde MM, Booth C, Kaye C, Hollison L.
    Am J Med Genet; 1985 Jul 10; 21(3):439-44. PubMed ID: 3895927
    [Abstract] [Full Text] [Related]

  • 13. Unilateral and asymmetric limb defects in man: delineation of the femur-fibula-ulna complex.
    Lenz W, Feldmann U.
    Birth Defects Orig Artic Ser; 1977 Jul 10; 13(1):269-85. PubMed ID: 851600
    [No Abstract] [Full Text] [Related]

  • 14. The EEC syndrome. Report of six patients.
    Pashayan HM, Pruzansky S, Solomon L.
    Birth Defects Orig Artic Ser; 1974 Jul 10; 10(7):105-27. PubMed ID: 4425508
    [No Abstract] [Full Text] [Related]

  • 15. [Popliteal pterygium syndrome. A exceptional case].
    Brun MF, Delcampe P, Retout A, Bachy B, Peron JM.
    Rev Stomatol Chir Maxillofac; 1994 Jul 10; 95(5):343-7. PubMed ID: 7984954
    [Abstract] [Full Text] [Related]

  • 16. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E, Clemens M.
    Am J Med Genet; 1996 Mar 01; 62(1):58-60. PubMed ID: 8779326
    [Abstract] [Full Text] [Related]

  • 17. Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsy.
    Loesch DZ, Hay DA, Sheffield LJ.
    Am J Med Genet; 1992 Nov 15; 44(5):543-50. PubMed ID: 1481805
    [Abstract] [Full Text] [Related]

  • 18. The Roberts syndrome.
    Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J.
    Birth Defects Orig Artic Ser; 1974 Nov 15; 10(5):87-95. PubMed ID: 4220010
    [Abstract] [Full Text] [Related]

  • 19. Poly-, syn- and oligodactylyl, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs--a new autosomal recessive syndrome.
    Fuhrmann W, Fuhrmann-Rieger A, de Sousa F.
    Eur J Pediatr; 1980 Mar 15; 133(2):123-9. PubMed ID: 7363910
    [Abstract] [Full Text] [Related]

  • 20. The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models.
    Gritli-Linde A.
    Curr Top Dev Biol; 2008 Mar 15; 84():37-138. PubMed ID: 19186243
    [Abstract] [Full Text] [Related]

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