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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

368 related items for PubMed ID: 4220010

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

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

  • 3. 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]

  • 4. 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 Oct 01; 12(5):201-8. PubMed ID: 953225
    [No Abstract] [Full Text] [Related]

  • 5. Autosomal recessive cleft lip/palate, ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family.
    Richieri-Costa A, Guion-Almeida ML, Freire-Maia N, Pinheiro M.
    Am J Med Genet; 1992 Sep 15; 44(2):158-62. PubMed ID: 1456284
    [Abstract] [Full Text] [Related]

  • 6. Roberts syndrome or "X-linked amelia"?
    Gershoni-Baruch R, Drugan A, Bronshtein M, Zimmer EZ.
    Am J Med Genet; 1990 Dec 15; 37(4):569-72. PubMed ID: 2260610
    [Abstract] [Full Text] [Related]

  • 7. Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome.
    Curry CJ, Hall BD.
    Birth Defects Orig Artic Ser; 1979 Dec 15; 15(5B):253-63. PubMed ID: 526581
    [No Abstract] [Full Text] [Related]

  • 8. Familial holoprosencephaly, heart defects, and polydactyly.
    Hennekam RC, van Noort G, de la Fuente AA.
    Am J Med Genet; 1991 Nov 01; 41(2):258-62. PubMed ID: 1785646
    [Abstract] [Full Text] [Related]

  • 9. Ophthalmo-acromelic syndrome.
    Le Merrer M, Nessmann C, Briard ML, Maroteaux P.
    Ann Genet; 1988 Nov 01; 31(4):226-9. PubMed ID: 3146242
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 29(4):901-8. PubMed ID: 3400735
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  • 12. 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]

  • 13. Familial broad terminal phalanges with one individual showing additional anomalies.
    Pavone L, Sorge G, Pavone V, Rizzo R, Ruggieri M, Polizzi A, Opitz JM.
    Am J Med Genet; 1997 Aug 22; 71(3):271-4. PubMed ID: 9268094
    [Abstract] [Full Text] [Related]

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  • 16. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Aug 22; 6(4):309-12. PubMed ID: 8775417
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  • 18. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
    Schrander-Stumpel C, de Die-Smulders C, Fryns JP, da Costa J, Bouckaert P.
    Am J Med Genet; 1990 Sep 22; 37(1):133-5. PubMed ID: 2240030
    [Abstract] [Full Text] [Related]

  • 19. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 22; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 20. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
    Bartsocas CS, Papas CV.
    J Med Genet; 1972 Jun 22; 9(2):222-6. PubMed ID: 4339984
    [No Abstract] [Full Text] [Related]

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