No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation

Clinical Genetics

Volumn 58, Issue 3, 2000, Pages 177-180

  Kotzot, D ^a   Lurie, I W ^b   Mehes K ^c   Werder, E ^a   Schinzel, A ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b Institute for Hereditary Diseases   (Belarus)

^c UNIVERSITY OF PÉCS   (Hungary)

Author keywords

Chromosomes 2, 6, 14, 16, 20, and 22; Intrauterine growth retardation; Primordial growth retardation; Silver Russell syndrome; Uniparental disomy

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 14; CHROMOSOME 16; CHROMOSOME 2; CHROMOSOME 20; CHROMOSOME 22; CHROMOSOME 6; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; HUMAN; INHERITANCE; INTRAUTERINE GROWTH RETARDATION; MALE; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

ADULT; ANEUPLOIDY; CHILD; CHROMOSOMES, HUMAN; FEMALE; FETAL GROWTH RETARDATION; GENETIC MARKERS; HAPLOTYPES; HUMANS; KARYOTYPING; MALE; MIDDLE AGED; PARENTS;

EID: 0033820253     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2000.580304.x     Document Type: Article

References (29)

1. Current concepts of fetal growth restriction: Part I. Causes, classification, and pathophysiology
2. Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients
3. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
4. A new genetic concept: Uniparental disomy and its potential effect, isodisomy
5. Abnormal phenotypes in uniparental disomy (UPD)-fundamental aspects and a critical review with bibliography of UPD other than 15
6. Uniparental maternal disomy 6 in a renal transplant patient
7. Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia
8. Genomic imprinting in mammals
9. Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22
10. Meiotic origin of trisomy in confined placental mosaicism correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction
11. Severe intra-uterine growth retardation in a patient with maternal uniparental disomy 22 and a 22-trisomic placenta
12. Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2)
13. Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea
14. Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia
15. The cell cycle control gene ZAC/PLAGL1 is imprinted - A strong candidate gene for transient neonatal diabetes
16. Maternal uniparental disomy 7 in Silver-Russell syndrome
17. Molecular studies in 37 Silver-Russell syndrome patients: Frequency and etiology of uniparental disomy
18. Cytogenetic and molecular studies in 32 Silver-Russell syndrome patients (SRS)
19. Search for candidate gene for Russell-Silver syndrome (RSS) on chromosome 17
20. Uniparental disomy and PEG1/MEST gene in Silver-Russell syndrome
21. Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7
22. Chromosome 7 uniparental disomy in Silver-Russell syndrome
23. Silver-Russell syndrome and exclusion of uniparental disomy
24. The incidence of uniparental disomy associated with intrauterine growth retardation in a cohort of thirty-five severely affected babies
25. Maternal uniparental disomy of chromosome 7 is confined to cases with Silver-Russell syndrome in children with growth retardation of unknown etiology
26. Uniparental disomy in congenital disorders: A prospective study
27. The contribution of uniparental disomy to congenital developmental defects in children born to ″old″ mothers
28. Trisomy first, translocation second, uniparental disomy and partial trisomy third: A new mechanism for complex chromosomal aneuploidy