Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants

Fathiya Al-Murshedi; Hassan Mirza; Abeer Al-Saegh; Maryam Al-Nabhani; Saud Al-Shabibi; Saleh Baawain; Amna Al-Futaisi; Wafaa Al-Shehhi; Almundher Al-Maawali

doi:10.1111/cge.13838

Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants

Fathiya Al-Murshedi, Hassan Mirza, Abeer Al-Saegh, Maryam Al-Nabhani, Saud Al-Shabibi, Saleh Baawain, Amna Al-Futaisi, Wafaa Al-Shehhi, Almundher Al-Maawali^*

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

2 Citations (Scopus)

Original language	English
Pages (from-to)	520-521
Number of pages	2
Journal	Clinical Genetics
Volume	98
Issue number	5
DOIs	https://doi.org/10.1111/cge.13838
Publication status	Published - Nov 1 2020

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/cge.13838

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@article{163cece2db784c518ebbfcd75ed366d1,

title = "Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants",

author = "Fathiya Al-Murshedi and Hassan Mirza and Abeer Al-Saegh and Maryam Al-Nabhani and Saud Al-Shabibi and Saleh Baawain and Amna Al-Futaisi and Wafaa Al-Shehhi and Almundher Al-Maawali",

note = "Funding Information: This work was supported by His Majesty Trust Funds at the Sultan Qaboos University; study code: SR/MED/GENT/16/01 ",

year = "2020",

month = nov,

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doi = "10.1111/cge.13838",

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volume = "98",

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T1 - Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants

AU - Al-Murshedi, Fathiya

AU - Mirza, Hassan

AU - Al-Saegh, Abeer

AU - Al-Nabhani, Maryam

AU - Al-Shabibi, Saud

AU - Baawain, Saleh

AU - Al-Futaisi, Amna

AU - Al-Shehhi, Wafaa

AU - Al-Maawali, Almundher

N1 - Funding Information: This work was supported by His Majesty Trust Funds at the Sultan Qaboos University; study code: SR/MED/GENT/16/01

PY - 2020/11/1

Y1 - 2020/11/1

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UR - http://www.scopus.com/inward/citedby.url?scp=85090458507&partnerID=8YFLogxK

U2 - 10.1111/cge.13838

DO - 10.1111/cge.13838

M3 - Letter

C2 - 32901920

AN - SCOPUS:85090458507

SN - 0009-9163

VL - 98

SP - 520

EP - 521

JO - Clinical Genetics

JF - Clinical Genetics

IS - 5

ER -

Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants

ASJC Scopus subject areas

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