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Journal Abstract Search

360 related items for PubMed ID: 9852671

  • 21. Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
    Mégarbané A, Choueiri R, Bleik J, Mezzina M, Caillaud C.
    J Med Genet; 1999 Aug; 36(8):637-40. PubMed ID: 10465117
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  • 22. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS, Wisniewski K, Brown WT.
    Am J Med Genet; 1994 Jul 15; 51(4):586-90. PubMed ID: 7943044
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  • 23. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA, García-Cruz D, García-Cruz O, Sánchez-Corona J.
    Am J Med Genet; 1995 Feb 13; 55(4):420-2. PubMed ID: 7762580
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  • 24. Dominant inheritance of holoprosencephaly.
    Cantú JM, Fragoso R, Garcia-Cruz D, Sánchez-Corona J.
    Birth Defects Orig Artic Ser; 1978 Feb 13; 14(6B):215-20. PubMed ID: 728563
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  • 30. An oculocerebrofacial syndrome.
    Kaufman RL, Rimoin DL, Prensky AL, Sly WS.
    Birth Defects Orig Artic Ser; 1971 Feb 13; 7(1):135-8. PubMed ID: 5006210
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  • 31. Familial holoprosencephaly.
    Dallaire L, Fraser FC, Wiglesworth FW.
    Birth Defects Orig Artic Ser; 1971 Jun 13; 7(7):136-42. PubMed ID: 5173201
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  • 33. 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 13; 15(1):29-34. PubMed ID: 17033686
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  • 36. Plantar lipomatosis, unusual facial phenotype and developmental delay: a new MCA/MR syndrome.
    Pierpont ME, Stewart FJ, Gorlin RJ.
    Am J Med Genet; 1998 Jan 06; 75(1):18-21. PubMed ID: 9450851
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  • 37. Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: a new syndrome.
    Mikati MA, Najjar SS, Sahli IF, Melhem RE, Mansour S, Der Kaloustian VM.
    Am J Med Genet; 1985 Nov 06; 22(3):599-608. PubMed ID: 2998187
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  • 38. Apparent Ruvalcaba syndrome with genitourinary abnormalities.
    Bialer MG, Wilson WG, Kelly TE.
    Am J Med Genet; 1989 Jul 06; 33(3):314-7. PubMed ID: 2679089
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  • 40. Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?
    Ioan DM, Fryns JP.
    Genet Couns; 2002 Jul 06; 13(3):353-6. PubMed ID: 12416645
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