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Journal Abstract Search

267 related items for PubMed ID: 953225

  • 1. 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; 12(5):201-8. PubMed ID: 953225
    [No Abstract] [Full Text] [Related]

  • 2. A syndrome of ankylosis, facial anomalies and pulmonary hypoplasia secondary to fetal neuromuscular dysfunction.
    Mease AD, Yeatman GW, Pettett G, Merenstein GB.
    Birth Defects Orig Artic Ser; 1976; 12(5):193-200. PubMed ID: 953224
    [No Abstract] [Full Text] [Related]

  • 3. Pulmonary hypoplasia, multiple ankyloses, and camptodactyly: one syndrome or some related forms?
    Lazjuk GI, Cherstvoy ED, Lurie IW, Nedzved MK.
    Helv Paediatr Acta; 1978 Apr; 33(1):73-9. PubMed ID: 669973
    [Abstract] [Full Text] [Related]

  • 4. Syndromes of camptodactyly, multiple ankylosis, facial anomalies, and pulmonary hypoplasia.
    Elias S, Boelen L, Simpson JL.
    Birth Defects Orig Artic Ser; 1978 Apr; 14(6B):243-51. PubMed ID: 728565
    [No Abstract] [Full Text] [Related]

  • 5. The Pena-Shokeir syndrome: report of five cases and further delineation of the syndrome.
    Chen H, Blumberg B, Immken L, Lachman R, Rightmire D, Fowler M, Bachman R, Beemer FA.
    Am J Med Genet; 1983 Oct; 16(2):213-24. PubMed ID: 6650566
    [Abstract] [Full Text] [Related]

  • 6. Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition.
    Pena SD, Shokeir MH.
    J Pediatr; 1974 Sep; 85(3):373-5. PubMed ID: 4431498
    [No Abstract] [Full Text] [Related]

  • 7. Syndrome of ankylosis, facial anomalies and pulmonary hypoplasia.
    Khan AA.
    Med J Zambia; 1977 Sep; 11(2):53-5. PubMed ID: 878635
    [Abstract] [Full Text] [Related]

  • 8. Syndrome of camptodactyly, ankyloses, facial anomalies, and pulmonary hypoplasia (Pena-Shokeir syndrome): obstetric and ultrasound aspects.
    Shenker L, Reed K, Anderson C, Hauck L, Spark R.
    Am J Obstet Gynecol; 1985 Jun 01; 152(3):303-7. PubMed ID: 3890548
    [Abstract] [Full Text] [Related]

  • 9. Fryns syndrome.
    Stratton RF, Young RS, Heiman HS, Carter JM.
    Am J Med Genet; 1993 Mar 01; 45(5):562-4. PubMed ID: 8456824
    [Abstract] [Full Text] [Related]

  • 10. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
    Froster UG, Rehder H, Höhn W, Oberheuser F.
    Am J Med Genet; 1993 Oct 01; 47(5):717-22. PubMed ID: 8267003
    [Abstract] [Full Text] [Related]

  • 11. The Roberts syndrome.
    Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J.
    Birth Defects Orig Artic Ser; 1974 Oct 01; 10(5):87-95. PubMed ID: 4220010
    [Abstract] [Full Text] [Related]

  • 12. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C, Jones KL, Saal HM, Stern HJ.
    Pediatrics; 1990 Apr 01; 85(4):499-504. PubMed ID: 2314962
    [Abstract] [Full Text] [Related]

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  • 14. Pathologic features in two siblings with the Pena-Shokeir I syndrome.
    Bisceglia M, Zelante L, Bosman C, Cera R, Dallapiccola B.
    Eur J Pediatr; 1987 May 01; 146(3):283-7. PubMed ID: 3595647
    [Abstract] [Full Text] [Related]

  • 15. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 May 01; 6(4):309-12. PubMed ID: 8775417
    [Abstract] [Full Text] [Related]

  • 16. Acute respiratory distress in Pena-Shokeir syndrome.
    Boesen PV, French CE.
    Ear Nose Throat J; 2004 Nov 01; 83(11):772-3. PubMed ID: 15628635
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Mesomelic limb shortness: a previously unreported autosomal recessive type.
    Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM.
    Am J Med Genet; 1993 Oct 01; 47(5):788-92. PubMed ID: 8267013
    [Abstract] [Full Text] [Related]

  • 19. 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]

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