Complete paternal uniparental isodisomy for Chromosome 2 revealed in a parentage testing case

Paternal isodisomy of chromosome 2 as a cause of long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency

(2010) Berivan Baskin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Polymorphism analysis and evaluation of nine non-CODIS STR loci in the Han population of Southern China

(2010) Da Yue Tong et al.   ANNALS OF HUMAN BIOLOGY

Genetic diversities of 21 non-CODIS autosomal STRs of a Chinese Tibetan ethnic minority group in Lhasa

(2010) Bo-feng Zhu et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Genetic variation analysis of 15 autosomal STR loci of AmpFℓSTR® Sinofiler™ PCR Amplification Kit in Henan (central China) Han population

(2010) Shuqin Huang et al.   Legal Medicine

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan

(2009) Matthew C. Keller et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Primary congenital glaucoma caused by the homozygous F261LCYP1B1mutation and paternal isodisomy of chromosome 2

(2009) M-P López-Garrido et al.   CLINICAL GENETICS

Polymorphism analysis of 15 STR loci in a large sample of the Han population in southern China

(2009) Dayue Tong et al.   Forensic Science International-Genetics

Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygousLRP2mutation due to complete chromosome 2 paternal isodisomy

(2008) Sibel Kantarci et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A paternity case with three genetic incompatibilities between father and child due to maternal uniparental disomy 21 and a mutation at the Y chromosome

(2008) Audrey Mansuet-Lupo et al.   Forensic Science International-Genetics