A variant in the LDL receptor-related protein encoding gene LRP4 underlying polydactyly and phalangeal synostosis in a family of Pakistani origin von Khan, Hammal, Ullah, Kifayat, Jan, Abid, Ali, Hamid, Ullah, Imran, Ahmad, Wasim

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In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis von Raza, Syed Irfan, Muhammad, Dost, Jan, Abid, Ali, Raja Hussain, Hassan, Mubashir, Ahmad, Wasim, Rashid, Sajid

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Sequence variants in GDF5 and TRPS1 underlie brachydactyly and tricho‐rhino‐phalangeal syndrome type III von Ullah, Asmat, Umair, Muhammad, Hussain, Shabir, Jan, Abid, Ahmad, Wasim

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A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment von Schrauwen, Isabelle, Chakchouk, Imen, Liaqat, Khurram, Jan, Abid, Nasir, Abdul, Hussain, Shabir, Nickerson, Deborah A., Bamshad, Michael J., Ullah, Asmat, Ahmad, Wasim, Leal, Suzanne M.

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Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families von Umair, Muhammad, Hassan, Annum, Jan, Abid, Ahmad, Farooq, Imran, Muhammad, Samman, Muhammad I, Basit, Sulman, Ahmad, Wasim

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Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein‐truncating mutations of ASPM von Hussain, Sadam, Nawaz, Amjad, Hamid, Malaika, Ullah, Waseem, Khan, Iqbal Nawaz, Afshan, Mehak, Rehman, Adil, Nawaz, Hamid, Halswick, Julia, Rehman, Shoaib‐ur, Ahmad, Sohail, Muzammal, Muhammad, Muhammad, Noor, Jan, Abid, Khan, Saadullah, Windpassinger, Christian, Khan, Muzammil Ahmad

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Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin von Khan, Niamatullah, Shah, Khadim, Fozia, Fozia, Khan, Sher A., Muhammad, Nazif, Nasir, Abdul, Ahmad, Ijaz, Rehman, Zia U., Jan, Abid, Muhammad, Noor, Khan, Saadullah

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Comments on: prevalence and risk factors for tuberculosis and HIV coinfections in Kenyan prison inmates von Hamza, Muhammad, Jalil, Zil-E-Huma, Sattar, Abid Jan Abdul, Sohail, Hamnah, Oduoye, Malik Olatunde

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Ellis–van Creveld syndrome and profound deafness resulted by sequence variants in the EVC / EVC2 and TMC1 genes von Umair, Muhammad, Seidel, Heide, Ahmed, Ishtiaq, Ullah, Asmat, Haack, Tobias B., Alhaddad, Bader, Jan, Abid, Rafique, Afzal, Strom, Tim M., Ahmad, Farooq, Meitinger, Thomas, Ahmad, Wasim

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The genetic cause of neurodevelopmental disorders in 30 consanguineous families von Paracha, Sohail Aziz, Nawaz, Shoaib, Tahir Sarwar, Muhammad, Shaheen, Asmat, Zaman, Gohar, Ahmed, Jawad, Shah, Fahim, Khwaja, Sundus, Jan, Abid, Khan, Nida, Kamal, Mohammad Azhar, Alam, Qamre, Abbas, Safdar, Farman, Saman, Waqas, Ahmed, Alkathiri, Afnan, Hamadi, Abdullah, Santoni, Federico, Ullah, Naseeb, Khalid, Bisma, Antonarakis, Stylianos E, Fakhro, Khalid A, Umair, Muhammad, Ansar, Muhammad

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Disease causing homozygous variants in the human hairless gene von Mehmood, Sabba, Jan, Abid, Raza, Syed Irfan, Ahmad, Farooq, Younus, Muhammad, Irfanullah, Shahi, Shamim, Ayub, Muhammad, Khan, Saadullah, Ahmad, Wasim

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A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre‐axial polydactyly von Ullah, Asmat, Umair, Muhammad, Majeed, Ayesha I., Abdullah, Jan, Abid, Ahmad, Wasim

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Novel mutations in PDE6A and CDHR1 cause retinitis pigmentosa in Pakistani families von Dawood, Muhammad, Lin, Siying, Din, Taj Ud, Shah, Irfan Ullah, Khan, Niamat, Jan, Abid, Marwan, Muhammad, Sultan, Komal, Nowshid, Maha, Tahir, Raheel, Ahmed, Asif Naveed, Yasin, Muhammad, Baple, Emma L, Crosby, Andrew H, Saleha, Shamim

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Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2 von Jan, Abid, Basit, Sulman, Wakil, Salma M, Ramzan, Khushnooda, Ahmad, Wasim

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Spectrofluorimetric Method for Quantification of Triazine Herbicides in Agricultural Matrices von MUHAMMAD, Mian, SHAH, Jasmin, JAN, M. Rasul, ARA, Behisht, KHAN, Mariam MAHABAT, JAN, Abid

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Frameshift Sequence Variants in the Human Lipase-H Gene Causing Hypotrichosis von Mehmood, Sabba, Shah, Sayed Hajan, Jan, Abid, Younus, Muhammad, Ahmad, Farooq, Ayub, Muhammad, Ahmad, Wasim

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Vortex-assisted liquid-liquid microextraction of selected non-steroidal anti-inflammatory drugs using supramolecular solvent von Jan, Abid, Shah, Jasmin, Jan, Muhammad Rasul

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Letter to the editor, “Superb microvascular ultrasound is a promising non-invasive diagnostic tool to assess a ventriculoperitoneal shunt system function: a feasibility study” von Abdul Sattar, Abid Jan, Hamza, Muhammad, Jalil, Zil E. Huma

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A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre‐axial polydactyly von Ullah, Asmat, Umair, Muhammad, Majeed, Ayesha I., Abdullah, Jan, Abid, Ahmad, Wasim

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FREQUENCY, DISTRIBUTION AND DETERMINANTS OF IRON DEFICIENCY ANEMIA AMONG THIRD TRIMESTER INDOOR PREGNANT WOMEN von Rehman, Asif, Malik, Farhat Rehana, Jan, Mir Abid, Zeb, Mahvash, Sabiha, Zia Ul Ain, Zafar, Danish, Shams, Saba, Khan, Beena

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