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Pubmed for Handhelds

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Journal Abstract Search

121 related items for PubMed ID: 7920642

  • 21. Genetic heterogeneity of familial hemiplegic migraine.
    Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR.
    Genomics; 1994 Jul 01; 22(1):21-6. PubMed ID: 7959770
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  • 22. A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.
    Bonnet D, Pelet A, Legeai-Mallet L, Sidi D, Mathieu M, Parent P, Plauchu H, Serville F, Schinzel A, Weissenbach J.
    Nat Genet; 1994 Apr 01; 6(4):405-8. PubMed ID: 8054983
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  • 23. A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.
    Deqaqi SC, N'Guessan M, Forner J, Sbiti A, Beldjord C, Chelly J, Sefiani A, Des Portes V.
    Ann Genet; 1998 Apr 01; 41(1):11-6. PubMed ID: 9599645
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  • 24. Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.
    Legius E, Schollen E, Matthijs G, Fryns JP.
    Eur J Hum Genet; 1998 Jan 01; 6(1):32-7. PubMed ID: 9781012
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  • 25. Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2.
    Faivre L, Mégarbané A, Alswaid A, Zylberberg L, Aldohayan N, Campos-Xavier B, Bacq D, Legeai-Mallet L, Bonaventure J, Munnich A, Cormier-Daire V.
    Hum Genet; 2002 Apr 01; 110(4):366-70. PubMed ID: 11941487
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  • 26. Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.
    Turner G, Gedeon A, Mulley J, Sutherland G, Rae J, Power K, Arthur I.
    Am J Med Genet; 1989 Dec 01; 34(4):463-9. PubMed ID: 2624253
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  • 29. X-linked mental retardation with dystonic movements of the hands (PRTS): revisited.
    Gedeon A, Partington M, Mulley J.
    Am J Med Genet; 1994 Jul 15; 51(4):565-8. PubMed ID: 7943040
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  • 30. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
    Martínez-Garay I, Tomás M, Oltra S, Ramser J, Moltó MD, Prieto F, Meindl A, Kutsche K, Martínez F.
    Eur J Hum Genet; 2007 Jan 15; 15(1):29-34. PubMed ID: 17033686
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  • 31. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
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  • 32. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
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  • 35. Mapping a gene for Noonan syndrome to the long arm of chromosome 12.
    Jamieson CR, van der Burgt I, Brady AF, van Reen M, Elsawi MM, Hol F, Jeffery S, Patton MA, Mariman E.
    Nat Genet; 1994 Dec 01; 8(4):357-60. PubMed ID: 7894486
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  • 37. The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.
    Paavola P, Salonen R, Weissenbach J, Peltonen L.
    Nat Genet; 1995 Oct 01; 11(2):213-5. PubMed ID: 7550354
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