## Abstract Fluorescence in situ hybridization (FISH) analyses were performed on six of seven patients who had been reported in 2004 to have an i(20q−) anomaly expressed as ider(20)(q10)del(20)(q11q13). The i(20q−) was investigated with a series of probes: a centromere‐specific probe for chromosome
A boy with 47,X,del(X)(p11→q13::q21→q24),del(Y)(q11)
✍ Scribed by Johannes Nielsen; Kirsten Rasmussen; Ingelise Sillesen
- Publisher
- Springer
- Year
- 1976
- Tongue
- English
- Weight
- 253 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
✦ Synopsis
Before the introduction of the banding technique we studied a boy presented as a case of 47, XX,?Yq-(Christensen and Nielsen, 1971). The case has been restudied with the use of different types of banding, which revealed the following karyotype 47, X,del(X)(p11 leads to q13::q21leads toq24), del(Y)(q11).
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