Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes? [5]

American Journal of Human Genetics

Volumn 61, Issue 2, 1997, Pages 461-462

  Shaffer, L G ^a   McCaskill, C ^a   Egli, C A ^a   Baker, J C ^a   Johnston, K M ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 2P; GENETIC MARKER; HUMAN; ISOCHROMOSOME; LETTER; MALE; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

EID: 0030856047     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0002-9297(07)64076-2     Document Type: Letter

References (5)

1. LE Bernard DK Kalousek S Langlois IJ Barrett WF Hansen AS Aylsworth DI Smith Confined placental mosaicism for trisomy 2 with fetal maternal uniparental disomy of chromosome 2 Am J Hum Genet Suppl 57 1995 A51
2. F Bernasconi A Karagüzel F Celep I Keser G Lüleci F Dutly AA Schinzel Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q) Am J Hum Genet 59 1996 1114 1118
3. K Harrison K Eisenger K Anyane-Yeboa S Brown Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture Am J Med Genet 58 1995 147 151
4. TH Nesbitt CL Bodine SG Kahler M Decker-Phillips Abnormal genital development in XY neonates associated with severe placental insufficiency and chronic intrauterine growth restriction Am J Hum Genet Suppl 59 1996 A40
5. AL Webb S Sturgiss P Warwicker SC Robson JA Goodship J Wolstenholme Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation Prenat Diagn 16 1996 958 962