Search Results - Alquaiti, Maha

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  1. 1
    Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects

    Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects by Hussein, Ibtessam R., Bader, Rima S., Chaudhary, Adeel G., Bassiouni, Randa, Alquaiti, Maha, Ashgan, Fai, Schulten, Hans-Juergen, Al Qahtani, Mohammad H.

    Published in Pediatric cardiology
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  2. 2
    Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) regions in hereditary non polyposis colorectal cancer (Lynch syndrome) in the Kingdom of Saudi Arabia

    Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) r... by Rasool, Mahmood, Pushparaj, Peter Natesan, Mirza, Zeenat, Imran Naseer, Muhammad, Abusamra, Heba, Alquaiti, Maha, Shaabad, Manal, Sibiany, Abdulrahman Mohamed Saeed, Gauthaman, Kalamegam, Al-Qahtani, Mohammed Hussein, Karim, Sajjad

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  3. 3
    Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi Arabia

    Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi A... by Hussein, Ibtessam Ramzi, Chaudhary, Adeel G, Bassiouni, Randa, AlQuaiti, Maha, Sogaty, Samira, Al-Qahtani, Mohammed

    Published in BMC genomics
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