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Showing 4 out of a total of 4 results for community: Medicine.
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Molecular diagnosis of Williams Buren syndrome in a cohort of Sri Lankan patients
Ranaweera, D.M.
;
de Silva, D.
;
Samarasinghe, D.
;
Perera, S.
;
Rajapaksha, N.
;
Chandrasekharan, N.V.
(
Sri Lanka Medical Association
,
2012
)
Meckel Gruber syndrome: a single gene cause of recurrent neural tube defects
de Silva, D.
;
Suriyawansa, D.
;
Mangalika, M.
;
Samarasinghe, D.
(
Sri Lanka Medical Association
,
2001
)
Molecular diagnosis of velo-cardio-facial syndrome among sri lankan patients with congenital cardiac defects
Tevarajan, I.
;
Ranaweera, D. M.
;
Perera, S.
;
Samarasinghe, D.
;
Morawakkorala, R.
;
Silva, R. L.
;
de Silva, D.
;
Chandrasekharan, N.V.
(
Sri Lanka College of Paediatricians
,
2015
)
Arterial tortuosity syndrome: A rare inherited form of connective tissue disorder with SLR2A10 gene mutation
Wijesinghe, S.
;
de Silva, D.
;
Samarasinghe, D.
;
Irugalbandara, S.
(
Sri Lanka College of Paediatricians
,
2022
)
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Author
de Silva, D. (4)
Samarasinghe, D. (4)
Chandrasekharan, N.V. (2)
Perera, S. (2)
Irugalbandara, S. (1)
Mangalika, M. (1)
Morawakkorala, R. (1)
Rajapaksha, N. (1)
Ranaweera, D. M. (1)
Ranaweera, D.M. (1)
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Subject
Molecular diagnosis (1)
Velo-cardio facial syndrome (1)
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Date Issued
2020 - 2022 (1)
2010 - 2019 (2)
2001 - 2009 (1)
Has File(s)
No (3)
Yes (1)