[Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods]. [electronic resource]
Producer: 19961210Description: 241-5 p. digitalISSN:- 0031-3939
- Abnormalities, Multiple -- genetics
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 22
- Craniofacial Abnormalities
- Cryptorchidism
- Cytogenetics -- methods
- Genetic Markers
- Heart Failure
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Intellectual Disability
- Male
- Translocation, Genetic -- genetics
- Trisomy -- diagnosis
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Publication Type: Case Reports; English Abstract; Journal Article; Research Support, Non-U.S. Gov't
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