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Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.

We report three unrelated patients with small terminal deletions involving 1p36.22-->pter that occurred de novo and compare our patients to the 10 previously reported cases. Although our patients have an identical cytogenetic deletion, patients 1 and 2 share similar clinical features that differ...

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Detaylı Bibliyografya
Asıl Yazarlar: Keppler-Noreuil, K M, Carroll, A J, Finley, W H, Rutledge, S L
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1995
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051636/
https://ncbi.nlm.nih.gov/pubmed/7473653
Etiketler: Etiketle
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