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Kriti D Khandelwal

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 22, 2013
Genomic approaches for studying craniofacial disordersKriti D Khandelwal, Hans van Bokhoven, Tony Roscioli, et al.
American Journal of Medical Genetics. Part A|May 18, 2017
Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemiaKriti D Khandelwal, Charlotte W Ockeloen, Hanka Venselaar, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesisCharlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 22, 2013
Genomic approaches for studying craniofacial disordersKriti D Khandelwal, Hans van Bokhoven, Tony Roscioli, et al.
American Journal of Medical Genetics. Part A|May 18, 2017
Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemiaKriti D Khandelwal, Charlotte W Ockeloen, Hanka Venselaar, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesisCharlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, et al.
Pageof 1