Yüklüyor......
Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24
Seckel syndrome (MIM 210600) is an autosomal recessive disorder of low birth weight, severe microcephaly, and dysmorphic facial appearance with receding forehead, prominent nose, and micrognathia. We have performed a genomic screen in two consanguineous families of Pakistani origin and found that th...
Kaydedildi:
| Asıl Yazarlar: | , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The American Society of Human Genetics
2000
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1287195/ https://ncbi.nlm.nih.gov/pubmed/10889046 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|