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Journal Abstract Search

198 related items for PubMed ID: 1776627

  • 1. New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.
    Seaver LH, Cassidy SB.
    Am J Med Genet; 1991 Dec 15; 41(4):405-9. PubMed ID: 1776627
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  • 2. Teebi hypertelorism syndrome.
    Koenig R.
    Clin Dysmorphol; 2003 Jul 15; 12(3):187-9. PubMed ID: 14564158
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  • 3. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV, Delp K.
    Clin Dysmorphol; 1994 Oct 15; 3(4):335-9. PubMed ID: 7894738
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  • 4. Aarskog syndrome: report of a family with review and discussion of nosology.
    Teebi AS, Rucquoi JK, Meyn MS.
    Am J Med Genet; 1993 Jun 15; 46(5):501-9. PubMed ID: 8322809
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  • 6. A new syndrome with distinct facial and auricular malformations and dominant inheritance.
    Simosa V, Penchaszadeh VB, Bustos T.
    Am J Med Genet; 1989 Feb 15; 32(2):184-6. PubMed ID: 2929657
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  • 9. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
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  • 10. Provisional new syndrome of MR/MCA with evolving phenotype.
    Lacassie Y, Morava E, LaMotta I.
    Am J Med Genet; 2002 Nov 22; 113(2):213-7. PubMed ID: 12407715
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  • 11. New dominant syndrome of pterygium colli, mental retardation, and digital anomalies.
    Khalifa MM, Graham G.
    Am J Med Genet; 1994 Aug 01; 52(1):55-7. PubMed ID: 7977463
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  • 13. 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 01; 26(2):481-91. PubMed ID: 3812597
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  • 15. Familial distal arthrogryposis with craniofacial abnormalities: a new subtype of type II?
    Moore CA, Weaver DD.
    Am J Med Genet; 1989 Jun 01; 33(2):231-7. PubMed ID: 2764034
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  • 16. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
    Wittwer B, Kircheisen R, Leutelt J, Orth U, Gal A.
    Am J Med Genet; 1996 Jul 12; 64(1):42-9. PubMed ID: 8826447
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