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Author/Creator Al‐Mamari, Watfa

1. Further phenotypic delineation of Alazami syndrome. Issue 8 (14th May 2022)

Authors:
Al‐Hinai, Abdulhamid; Al‐Hashmi, Samiya; Ganesh, Anuradha; Al‐Hashmi, Nadia; Al‐Saegh, Abeer; Al‐Mamari, Watfa; Al‐Murshedi, Fathiya; Al‐Thihli, Khalid; Al‐Kindi, Adila; Al‐Maawali, Almundher
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 8(2022)
Page Start:
2485
Record Type:
Journal Article
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2. Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. Issue 7 (5th May 2016)

Authors:
Al‐Amri, Ahmed; Saegh, Abeer Al; Al‐Mamari, Watfa; El‐Asrag, Mohammed E.; Ivorra, Jose L.; Cardno, Alastair G.; Inglehearn, Chris F.; Clapcote, Steven J.; Ali, Manir
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 7(2016)
Page Start:
1826
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits. Issue 6 (12th September 2018)

Authors:
Al‐Nabhani, Maryam; Al‐Rashdi, Samiya; Al‐Murshedi, Fathiya; Al‐Kindi, Adila; Al‐Thihli, Khalid; Al‐Saegh, Abeer; Al‐Futaisi, Amna; Al‐Mamari, Watfa; Zadjali, Fahad; Al‐Maawali, Almundher
Journal:
Clinical genetics
Issue:
Volume 94:Issue 6(2018)
Page Start:
495
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗