A. Al-Kindy

发表

Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman

Z. Bruwer, U. Achandira, Khalsa Al Kharousi, 2014, Journal of Genetic Counseling.

Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population

K. Al-Thihli, Z. Bruwer, A. Al-Kindy, 2015, Journal of Autism and Developmental Disorders.

Coffin–Siris syndrome is a SWI/SNF complex disorder

N. Matsumoto, Y. Makita, H. Ohashi, 2014, Clinical genetics.

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

F. Alkuraya, E. Faqeih, K. Al-Thihli, 2017, Human Genetics.

One in three: congenital bent bone disease and intermittent hyperthermia in three siblings with stuve-wiedemann syndrome.

R. Koul, A. Al-Futaisi, A. Al-Kindy, 2013, Sultan Qaboos University medical journal.

Constitutional trisomy 8 mosaicism syndrome: case report and review

A. Al-Kindy, A. M. Udayakumar, 2013, Journal of Pediatric Genetics.

Microphthalmos-anophthalmos-coloboma (MAC) spectrum in two brothers with Renpenning syndrome due to a truncating mutation in the polyglutamine tract binding protein 1 (PQBP1) gene

A. Ganesh, A. Al-Kindy, Maha Mameesh, 2019, Ophthalmic genetics.

Macro and microclimate effects on cover zone properties of field cured concrete

Adil Al-Kindy, A. Al-Kindy, 1998 .

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

F. Alkuraya, E. Faqeih, K. Al-Thihli, 2017, Human Genetics.

Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population

Z. Bruwer, Khalid Al-Thihli, A. Al-Kindy, 2015, Journal of Autism and Developmental Disorders.

A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome

A. Al-Kindy, A. M. Udayakumar, 2013, Journal of Pediatric Genetics.

Erratum to: Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman

Z. Bruwer, Khalsa Al Kharousi, A. Al-Kindy, 2015, Journal of Genetic Counseling.

De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism.

A. Al-Kindy, Watfa S Al-Mamari, A. M. Udayakumar, 2015, Sultan Qaboos University medical journal.

One in three: congenital bent bone disease and intermittent hyperthermia in three siblings with stuve-wiedemann syndrome.

R. Koul, A. Al-Futaisi, A. Al-Kindy, 2013, Sultan Qaboos University medical journal.