De Vries, BB; Knight, SJ; Homfray, T; Smithson, SF; Flint, J; Winter, RM
(2001)
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?
JOURNAL OF MEDICAL GENETICS, 38 (3).
175 - 178 (4).
ISSN 0022-2593
https://doi.org/10.1136/jmg.38.3.175
SGUL Authors: Homfray, Tessa
Full text not available from this repository.
| Item Type: |
Article
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| Additional Information: |
PubMed ID: 11303509 |
| Keywords: |
Abnormalities, Multiple, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 1, Family Health, Fatal Outcome, Female, Fetus, Humans, In Situ Hybridization, Fluorescence, Intellectual Disability, Male, Phenotype, Telomere, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, IDIOPATHIC MENTAL-RETARDATION, DISTAL LONG ARM, CHROMOSOMAL REARRANGEMENTS, TELOMERES, CHILDREN, FISH |
| Journal or Publication Title: |
JOURNAL OF MEDICAL GENETICS |
| ISSN: |
0022-2593 |
| Related URLs: |
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| Dates: |
| Date | Event |
|---|
| 1 March 2001 | Published |
|
| Web of Science ID: |
WOS:000167470000006 |
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| URI: |
https://openaccess.sgul.ac.uk/id/eprint/480 |
| Publisher's version: |
https://doi.org/10.1136/jmg.38.3.175 |
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