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Journal Abstract Search

87 related items for PubMed ID: 2090119

  • 1. Geleophysic dysplasia.
    Wraith JE, Bankier A, Chow CW, Danks DM, Sardharwalla IB.
    Am J Med Genet; 1990 Feb; 35(2):153-6. PubMed ID: 2090119
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  • 7. Phenotypic variability in children with growth hormone deficiency associated with posterior pituitary ectopia.
    Simon D, Hadjiathanasiou C, Garel C, Czernichow P, Léger J.
    Clin Endocrinol (Oxf); 2006 Apr; 64(4):416-22. PubMed ID: 16584514
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  • 9. Melnick-Needles syndrome: indication for an autosomal recessive form.
    ter Haar B, Hamel B, Hendriks J, de Jager J.
    Am J Med Genet; 1982 Dec; 13(4):469-77. PubMed ID: 7158646
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  • 10. Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate form.
    Titomanlio L, Della Casa R, Lecora M, Farina V, Sebastio G, Andria G, Parenti G.
    Am J Med Genet; 1999 Sep 03; 86(1):82-5. PubMed ID: 10440835
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  • 13. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Sep 03; 6(4):309-12. PubMed ID: 8775417
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  • 16. Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?
    Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G.
    Am J Med Genet; 1993 Aug 15; 47(2):299-302. PubMed ID: 8213924
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  • 18. Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family.
    Mégarbané A, Delague V, Salem N, Loiselet J.
    Am J Med Genet; 1999 Nov 05; 87(1):88-90. PubMed ID: 10528257
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  • 20. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Miny P, Lenz W.
    Am J Med Genet; 1985 Jun 05; 21(2):317-24. PubMed ID: 4014313
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