Detection of chromosome aberrations during prenatal genetic testing for single gene disorders [2]

Prenatal Diagnosis

Volumn 24, Issue 11, 2004, Pages 924-925

  Chen, Chih Ping ^a,b   Lin, Shuan Pei ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALPHA THALASSEMIA; ANEUPLOIDY; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; FEMALE; FETUS; HUMAN; LETTER; MUCOLIPIDOSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ROBERTSONIAN CHROMOSOME TRANSLOCATION; TRISOMY 18; TRISOMY 21;

ADULT; ALPHA-THALASSEMIA; CHROMOSOME ABERRATIONS; DIAGNOSIS, DIFFERENTIAL; FEMALE; FETAL DEATH; GENETIC TECHNIQUES; HUMANS; INFANT, NEWBORN; MALE; MUCOLIPIDOSES; PREGNANCY; PREGNANCY TRIMESTER, FIRST; PREGNANCY TRIMESTER, SECOND; PRENATAL DIAGNOSIS; TWINS;

ROBERTSONIA;

EID: 9644302505     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.953     Document Type: Letter

References (5)

1. Alpman A, Bora E, Karaca E, et al. 2004. Detection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease. Genet Counsel 15: 99-100.
2. Berned SA, Horwitz J, McCaskill C, Shaffer LG. 2000. Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes. Am J Hum Genet 66: 1787-1793.
3. Chao M-C, Yang S-Y, Chang Y, et al. 2001. Prenatal diagnosis of der(11)t(11;18)(q24;q21.3) due to paternal balanced translocation and both parents are carriers of α-thalassemia-1-a case report. Kaohsiung J Med Sci 17: 430-436.
4. Chen M, Yeh G-P, Shih J-C, Wang B-T. 2004. Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy. Prenat Diagn 24: 137-143.
5. Gardner RJM, Sutherland GR (eds). 2004. Chromosome Abnormalities and Genetic Counseling (3rd edn), Oxford University Press: New York; 122-137.