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You searched for: Author/Creator Haaf, T- Haaf, T [remove] 5
- 616.042 4
- Medical genetics -- Periodicals 4
- 618 1
- CTHD, conotruncal heart defects -- VCFS, velocardiofacial syndrome -- DGS, DiGeorge syndrome -- CTAFS, conotruncal anomaly-face syndrome -- TOF, tetralogy of Fallot 1
- FISH, fluorescence in situ hybridisation -- OFC, occipito-frontal head circumference -- RACE, rapid amplification of cDNA ends 1
- Human reproduction -- Periodicals 1
- chromosomal translocation -- fluorescence in situ hybridisation (FISH) -- Mendelian Cytogenetics Network (MCN) -- mental retardation (MR) 1
- chromosome breakpoint -- de novo translocation -- developmental delay -- recurrent infections -- TCBA1 gene 1
- conotruncal heart defects -- 22q11 deletion -- 10p13-14 deletion 1
- nucleolus organiser region -- non-acrocentric chromosome -- 4qs -- NOR insertion 1