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Search Results - Al-Kharusi, Khalsa
Search Results - Al-Kharusi, Khalsa
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The experience of Preimplantation Genetic Testing (PGT) among Muslim couples in Oman in the Middle East
by
Al‐Kharusi, Khalsa
,
Bruwer, Zandre
,
Wessels, Tina‐Marié
Published in
Journal of genetic counseling
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Deficiency of acyl‐CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset
by
Al‐Thihli, Khalid
,
Afting, Cassian
,
Al‐Hashmi, Nadia
,
Mohammed, Mohammed
,
Sliwinski, Svenja
,
Al Shibli, Naema
,
Al‐Said, Khoula
,
Al‐Kasbi, Ghalia
,
Al‐Kharusi, Khalsa
,
Merle, Uta
,
Füllekrug, Joachim
,
Al‐Maawali, Almundher
Published in
Clinical genetics
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The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families
by
Al-Kasbi, Ghalia
,
Al-Murshedi, Fathiya
,
Al-Kindi, Adila
,
Al-Hashimi, Nadia
,
Al-Thihli, Khalid
,
Al-Saegh, Abeer
,
Al-Futaisi, Amna
,
Al-Mamari, Watfa
,
Al-Asmi, Abdullah
,
Bruwer, Zandre
,
Al-Kharusi, Khalsa
,
Al-Rashdi, Samiya
,
Zadjali, Fahad
,
Al-Yahyaee, Said
,
Al-Maawali, Almundher
Published in
Scientific reports
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Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 Disease
by
Al-Murshedi , Fathiya
,
Bruwer , Zandre
,
Al-Kharusi , Khalsa
,
Meftah , Douja
,
Scott , Patrick
Published in
Oman medical journal
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Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period
by
Bruwer, Zandré
,
Al Ubaidani, Salwa
,
Al Kharusi, Khalsa
,
Al Murshedi, Fathiya
,
Al-Maawali, Almundher
,
Al Sayegh, Abeer
,
Al Kindy, Adila
,
Al Riyami, Nihal
,
Al Dughaishi, Tamima
,
Al Salmani, Mouza
,
Al Hashmi, Nadia
,
Al Shehhi, Maryam
,
Al Fahdi, Badriya
,
Al Amri, Sumaya
,
Al-Thihli, Khalid
Published in
Journal of community genetics
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Genetic counseling development and milestone in Oman
by
Al-Kharusi, Khalsa
,
Van Wyk, Chantel
,
Al Hinai, Mariya
,
Al-Fori, Amel
,
Bruwer, Zandre
Published in
Genetics in Medicine Open
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Biallelic loss-of-function variants of GFRA1 cause lethal bilateral renal agenesis
by
Al-Shamsi, Bushra
,
Al-Kasbi, Ghalia
,
Al-Kindi, Adila
,
Bruwer, Zandre
,
Al-Kharusi, Khalsa
,
Al-Maawali, Almundher
Published in
European journal of medical genetics
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IDENTIFICATION OF PROGNOSIS MARKERS IN PEDIATRIC HIGH-RISK ACUTE LYMPHOBLASTIC LEUKEMIA
by
Al-Lamki, Zakia
,
Wali, Yasser A.
,
Wasifuddin, Shah M.
,
Zachariah, Mathew
,
Al-Mjeni, Rayhanah
,
Li, Changping
,
Muralitharan, Shanmugakonar
,
Al-Kharusi, Khalsa
,
Gunaratne, Preethi
,
Peterson, Leif
,
Gibbs, Richard
,
Gingras, Marie-Claude
,
Margolin, Judith F.
Published in
Pediatric hematology and oncology
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Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 Disease
by
Scott, Patrick
,
Bruwer, Zandre
,
Al-Kharusi, Khalsa
,
Meftah, Douja
,
Al-Murshedi, Fathiya
Published in
Oman medical journal
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