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Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?

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

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Item Type: Article
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
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Dates:
DateEvent
1 March 2001Published
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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