Genotype-phenotype correlation in Bardet-Biedl Syndrome

Genotype-phenotype correlation in Bardet-Biedl Syndrome

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Forsythe, E, Sparks, K, Huda, M, Hazlehurst, J, Muajhid, S, Carroll, P, McGowan, B, Tomlinson, J, Mohammed, S, Beales, P
Μορφή:	Conference item
Έκδοση:	2012

Παρόμοια τεκμήρια

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ανά: Omer Ali Mohamed Ahmed Elawad, κ.ά.
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ανά: Natacha Sloboda, κ.ά.
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Έκδοση: (2015-09-01)

A Case Report on the Bardet Biedl Syndrome with Hypokalaemic Paralysis
ανά: Prasanth Y.M., κ.ά.
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Caregiver burden in Bardet-Biedl syndrome: findings from the CARE-BBS study
ανά: Elizabeth Forsythe, κ.ά.
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Computational and Structural Analysis to Assess the Pathogenicity of Bardet-Biedl Syndrome Related Missense Variants Identified in Bardet-Biedl Syndrome 10 Gene (BBS10)
ανά: Neha Gupta, κ.ά.
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ανά: Ena Arora, MD, κ.ά.
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