Deletion (12)(q15q21.2)

The infant who is the subject of this report is, to the author's knowledge, the second reported case with a deletion, interstitial or terminal, of the long arm of chromosome 12. The patient was a three and a half month old white female. She was the product of an uncomplicated term pregnancy and...

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Veröffentlicht in:Journal of medical genetics 1989-05, Vol.26 (5), p.343-344
Hauptverfasser: Watson, M S, McAllister-Barton, L, Mahoney, M J, Breg, W R
Format: Artikel
Sprache:eng
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Zusammenfassung:The infant who is the subject of this report is, to the author's knowledge, the second reported case with a deletion, interstitial or terminal, of the long arm of chromosome 12. The patient was a three and a half month old white female. She was the product of an uncomplicated term pregnancy and normal spontaneous vaginal delivery to a 32 year old, G2P1, healthy mother and a 40 year old healthy father. Birth weight was 3300 g. Paternal history was significant for a child with Potter's syndrome from an earlier marriage.
ISSN:0022-2593
1468-6244
1468-6244
DOI:10.1136/jmg.26.5.343