kw.\*:("HEXADACTYLIE")
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A NEW CASE OF TRISOMY FOR THE DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9;13) (P21;Q21).JOTTERAND M; JUILLARD E.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 213-222; BIBL. 20 REF.Article
Oreillette unique et héxadactylie : A propos d'une observation = Single atrium and hexadactyly: About a case reportHADDOUR, L; HADDOUR, N; DOGHMI, N et al.Maghreb médical. 2005, Num 372, pp 46-47, issn 0330-258X, 2 p.Article
De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformationsYING YUE; FARCAS, Ruxandra; HAAF, Thomas et al.European journal of human genetics. 2007, Vol 15, Num 5, pp 570-577, issn 1018-4813, 8 p.Article
Multicolor banding detects a complex three chromosome, seven breakpoint unbalanced rearrangement in an ICSI-derived fetus with multiple abnormalitiesSELLER, Mary J; BINT, Susan; KAVALIER, Fred et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 10, pp 1102-1107, issn 1552-4825, 6 p.Article