These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 3189394)

  • 1. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
    Saal HM; Greenstein RM; Weinbaum PJ; Poole AE
    Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive Robinow syndrome.
    Teebi AS
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A; Pereira SC
    Am J Med Genet; 1992 Mar; 42(5):681-7. PubMed ID: 1632438
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?
    Moog U; Bleeker-Wagemakers EM; Crobach P; Vles JS; Schrander-Stumpel CT
    Am J Med Genet; 1998 Jul; 78(3):263-6. PubMed ID: 9677063
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM; Winter RM
    Am J Med Genet; 1988 Jul; 30(3):719-24. PubMed ID: 3055984
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
    Koiffmann CP; Wajntal A; Huyke BJ; Castro RM
    Am J Med Genet; 1988 Feb; 29(2):263-8. PubMed ID: 3354597
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.
    Cerqueira DF; de Souza IP
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Mar; 105(3):353-7. PubMed ID: 18061493
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.
    Richieri-Costa A; Pereira SC
    Am J Med Genet; 1993 Oct; 47(5):707-9. PubMed ID: 8267000
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital hypothyroidism in Peters plus syndrome.
    Kosaki R; Kamiishi A; Sugiyama R; Kawai M; Hasegawa T; Kosaki K
    Ophthalmic Genet; 2006 Jun; 27(2):67-9. PubMed ID: 16754209
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.
    Toriello HV; Higgins JV; Miller T
    Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 37(1):133-5. PubMed ID: 2240030
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
    Toriello HV; Carey JC
    Am J Med Genet; 1988 Sep; 31(1):17-23. PubMed ID: 3223497
    [TBL] [Abstract][Full Text] [Related]  

  • 14. PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects.
    Powell CM; Chandra RS; Saal HM
    Am J Med Genet; 1993 Nov; 47(6):807-11. PubMed ID: 8279476
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
    Temtamy SA; Shoukry AS; Raafat M; Mihareb S
    Birth Defects Orig Artic Ser; 1975; 11(2):104-8. PubMed ID: 1227520
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 47(5):788-92. PubMed ID: 8267013
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
    Ritscher D; Schinzel A; Boltshauser E; Briner J; Arbenz U; Sigg P
    Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two unrelated children with developmental delay, short stature and anterior chamber cleavage disorder, cerebellar hypoplasia, endocrine disturbances and tracheostenosis: a new entity?
    Jung C; Wolff G; Back E; Stahl M
    Clin Dysmorphol; 1995 Jan; 4(1):44-51. PubMed ID: 7537583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance.
    Aymé S; Mattei JF
    Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Report of a case and further delineation of the SHORT syndrome.
    Toriello HV; Wakefield S; Komar K; Higgins JV; Waterman DF
    Am J Med Genet; 1985 Oct; 22(2):311-4. PubMed ID: 4050863
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.