KATE, SUDAM L. and YEOLA, GUNVANT H. and DALVI, PRASHANT N. and KULKARNI, GIRISH T. and PRABHUNE, YOGESH S. and MANCHANDA, RUMA V. (2017) SICKLE CELL DISORDER: A FAMILY STUDY WITH EIGHT HOMOZYGOUS AND TWO HETEROZYGOUS CHILDREN. BIONATURE, 37 (2). pp. 67-71.
![[thumbnail of 37_2-2.pdf]](http://library.eprintglobalarchived.com/style/images/fileicons/text.png)
Text
37_2-2.pdf - Published Version
Download (191kB)
Abstract
Sickle cell anaemia is a universal haemoglobin genetic disorder exhibiting segregation in many families but according to our find, this large family of eight homozygous cases, is the largest single family reported in the world literature.
| Item Type: | Article |
|---|---|
| Subjects: | Middle Asian Archive > Biological Science |
| Depositing User: | Managing Editor |
| Date Deposited: | 06 Jul 2024 08:00 |
| Last Modified: | 06 Jul 2024 08:00 |
| URI: | http://library.eprintglobalarchived.com/id/eprint/1120 |
Actions (login required)
- View Item