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Journal Abstract Search

155 related items for PubMed ID: 7545871

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  • 4. Interstitial deletion of the long arm of chromosome 3: case report, review, and definition of a phenotype.
    Alvarado M, Bocian M, Walker AP.
    Am J Med Genet; 1987 Aug; 27(4):781-6. PubMed ID: 3122568
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  • 5. Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndrome.
    Casteels I, Devriendt K, Van Cleynenbreugel H, Demaerel P, De Tavernier F, Fryns JP.
    Br J Ophthalmol; 2001 Apr; 85(4):499-500. PubMed ID: 11302131
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  • 6. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
    Taysi K, Sekhon GS, Hillman RE.
    Am J Med Genet; 1982 Dec; 13(4):423-30. PubMed ID: 7158642
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  • 7. De novo deletion of chromosome 11q13.4-q14.3 in a boy with microcephaly, ptosis and developmental delay.
    Wincent J, Schoumans J, Anderlid BM.
    Eur J Med Genet; 2010 Dec; 53(1):50-3. PubMed ID: 19857611
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  • 9. A genetic association between microcephaly and lymphedema.
    Meinecke P.
    Am J Med Genet; 1987 Jan; 26(1):233. PubMed ID: 3812570
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  • 13. Blepharophimosis sequence (BPES) and microcephaly in a girl with del(3) (q22.2q23): a putative gene responsible for microcephaly close to the BPES gene?
    Ishikiriyama S, Goto M.
    Am J Med Genet; 1993 Sep 15; 47(4):487-9. PubMed ID: 8256811
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  • 16. Concurrence of inv(7)(q11.2q32) and del(8)(p23.1) in a girl with congenital microcephaly, hypotonia, developmental delay, strabismus, hypernatremia, hypermagnesemia and deafness.
    Mahjoubi F, Nasiri F, Razazian F.
    Genet Couns; 2012 Sep 15; 23(3):397-404. PubMed ID: 23072189
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  • 18. Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature.
    Eventov-Friedman S, Singer A, Shinwell ES.
    Acta Paediatr; 2009 Apr 15; 98(4):758-9. PubMed ID: 19076985
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