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Table 1 STR analysis of patient and her parents

From: Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder

Marker

Position

Subject

Genotype

Inheritance

D13S175

1,653,855

Patient

1/1

Homozygous, P

  

Father

1/2

 
  

Mother

3/4

 

D13S171

14,064,951

Patient

1/1

Homozygous, M or P

  

Father

1/1

 
  

Mother

1/2

 

D13S218

19,831,225

Patient

1/1

Homozygous, M or P

  

Father

1/2

 
  

Mother

1/1

 

D13S155

34,882,886

Patient

1/1

Homozygous, M or P

  

Father

1/2

 
  

Mother

1/3

 

D13S176

41,205,385

Patient

1/1

Homozygous, P

  

Father

1/2

 
  

Mother

1/3

 

D13S71

75,575,535

Patient

1/1

Homozygous, P

  

Father

1/1

 
  

Mother

2/2

 

D13S154

76,860,260

Patient

1/1

Homozygous, P

  

Father

1/2

 
  

Mother

3/4

 

D13S174

102,954,076

Patient

1/1

Homozygous, M or P

  

Father

1/2

 
  

Mother

1/3

 

D13S1809

106,132,754

Patient

1/1

Homozygous, P

  

Father

1/2

 
  

Mother

2/3

 

D13S173

107,806,947

Patient

1/1

Homozygous, M or P

  

Father

1/2

 
  

Mother

1/1

 

D13S1265

109,328,688

Patient

1/1

Homozygous, P

  

Father

1/2

 
  

Mother

2/3

 

D13S1295

113,094,472

Patient

1/1

Homozygous, M or P

  

Father

1/2

 
  

Mother

1/1

 

D21S270

 

Patient

1/2

 
  

Father

1/2

 
  

Mother

2/3

 
  1. Chromosome 13 and 21 markers, along with position on chromosome (ensembl.org). Alleles were assigned arbitrary numbers, and genotype information is given for the patient and parents. Inheritance patterns have been determined. P indicates paternal inheritance and M indicates maternal inheritance. Bolded inheritance patterns demonstrate the expression of a single paternal allele and no maternal alleles in the patient, when the father is heterozygous.
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Molecular Cytogenetics

ISSN: 1755-8166