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Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome.
Authors: Semerci, C. Nur; Cinbis, Mine; Ullmann, Reinhard; Steininger, Anne; Bahce, Muhterem; Yagci, Baki; Ozden, Serap; Sabir, Nuran; Gumus, Dilihan; Tepeli, Emre; Arteaga, Jazmín; Mutchinick, Osvaldo M.
Date of Publication (YYYY-MM-DD): 2010-05-27
Title of Journal: American Journal of Medical Genetics Part A
Volume: 152A
Issue / Number: 7
Start Page: 1724
End Page: 1729
Document Type: Article
ID: 534116.0
 
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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
Authors: Kirov, George; Gumus, Dilihan; Chen, Wei; Norton, Nadine; Georgieva, Lyudmila; Sari, Murat; O’Donovan, Michael C.; Erdogan, Fikret; Owen, Michael J.; Ropers, Hans-Hilger; Ullmann, Reinhard
Date of Publication (YYYY-MM-DD): 2008-03-01
Title of Journal: Human Molecular Genetics
Volume: 17
Issue / Number: 3
Start Page: 458
End Page: 465
Document Type: Article
ID: 408444.0
 
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Entries: 1-2  
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