Author/Creator: Mory, A. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Mory, A.

1. Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies. (1st July 2022)

Authors:: Yaron, Y.; Ofen Glassner, V.; Mory, A.; Zunz Henig, N.; Kurolap, A.; Bar Shira, A.; Brabbing Goldstein, D.; Marom, D.; Ben Sira, L.; Baris Feldman, H.; Malinger, G.; Krajden Haratz, K.; Reches, A.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 60:Number 1(2022)
Page Start:: 59
Record Type:: Journal Article
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2. Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita. Issue 1 (20th January 2016)

Authors:: Ekhilevitch, N.; Kurolap, A.; Oz‐Levi, D.; Mory, A.; Hershkovitz, T.; Ast, G.; Mandel, H.; Baris, H.N.
Journal:: Clinical genetics
Issue:: Volume 90:Issue 1(2016)
Page Start:: 84
Record Type:: Journal Article
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3. The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews. Issue 9 (September 2015)

Authors:: Dagan, E.; Schlesinger, I.; Ayoub, M.; Mory, A.; Nassar, M.; Kurolap, A.; Peretz-Aharon, J.; Gershoni-Baruch, R.
Journal:: Parkinsonism & related disorders
Issue:: Volume 21:Issue 9(2015)
Page Start:: 1067
Record Type:: Journal Article
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