Consanguinity and reproductive health among Arabs von Tadmouri, Ghazi O, Nair, Pratibha, Obeid, Tasneem, Al Ali, Mahmoud T, Al Khaja, Najib, Hamamy, Hanan A

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Parental decisions following the prenatal diagnosis of sex chromosome abnormalities von Hamamy, Hanan A, Dahoun, Sophie

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Epidemiological profile of common haemoglobinopathies in Arab countries von Hamamy, Hanan A., Al-Allawi, Nasir A. S.

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First Report of Clinical, Functional, and Molecular Investigation of Chronic Granulomatous Disease in Nine Jordanian Families von Bakri, Faris G, Martel, Cécile, Khuri-Bulos, Najwa, Mahafzah, Azmi, El-Khateeb, Mohammad S, Al-Wahadneh, Adel M, Hayajneh, Wail A, Hamamy, Hanan A, Maquet, Elisabeth, Molin, Michelle, Stasia, Marie José

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Severe hypertelorism, midface prominence, prominent/simple ears, severe myopia, borderline intelligence, and bone fragility in two brothers: New syndrome? von Hamamy, Hanan A., Teebi, Ahmad S., Oudjhane, Kamaldine, Shegem, N.N., Ajlouni, K.M.

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Consanguinity and genetic disorders : Profile from Jordan von HAMAMY, Hanan A, MASRI, Amira T, AL-HADIDY, Azmy M, AJLOUNI, Kamel M

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Clinical and Inheritance Profiles of Hyperekplexia in Jordan von Masri, Amira Taher, Hamamy, Hanan A.

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Clinical and inheritance profiles of Kallmann syndrome in Jordan von Abujbara, Mousa A, Hamamy, Hanan A, Jarrah, Nadim S, Shegem, Nadima S, Ajlouni, Kamel M

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Pituitary enlargement in patients with primary hypothyroidism von Khawaja, Nahla M, Taher, Bassam M, Barham, Muries E, Naser, Abeer A, Hadidy, Azmy M, Ahmad, Azmi T, Hamamy, Hanan A, Yaghi, Nakhleh A, Ajlouni, Kamel M

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Hereditary multiple exostoses with pseudoaneurysm von Al-Hadidy, Azmy M, Al-Smady, Moa'ath M, Haroun, Azmi A, Hamamy, Hanan A, Ghoul, Suha M, Shennak, Akram O

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Male transient hip osteoporosis: are physicians at a higher risk? von Hadidy, Azmy M., Al Ryalat, Nosaiba T., Hadidi, Shaher T., Tarawneh, Emad S., Hadidi, Maher T., Samara, Osama A., Abu-Labn, Deema M., Al-Rousan, Lawrence M., Hiyasat, Dana A., Hamamy, Hanan A.

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Precocious puberty revealing severe hypothyroidism von TAHER, Bassam M, HAMAMY, Hanan A, NINO, Marlin I, AJLOUNI, Kamel M

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Cockayne syndrome in 2 siblings von HAMAMY, Hanan A, DAAS, Hanady A, SHEGEM, Nadima S, AL-HADIDY, Azmy M, AFLOUNI, Kamel M

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Consanguinity and Reproductive Health in Iraq von Hamamy, Hanan A., AL-Hakkak, Zuhair S.

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Glucose-6-phosphate dehydrogenase deficiency in Iraq von Hamamy, H A, Saeed, T K

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Consanguineous marriages: Preconception consultation in primary health care settings von Hamamy, Hanan

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Consanguinity and Dysmorphology in Arabs von Al-Gazali, Lihadh, Hamamy, Hanan

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Genetic disorders in the Arab world von Al-Gazali, Lihadh, Hamamy, Hanan, Al-Arrayad, Shaikha

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INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex von Mascibroda, Lauren G., Shboul, Mohammad, Elrod, Nathan D., Colleaux, Laurence, Hamamy, Hanan, Huang, Kai-Lieh, Peart, Natoya, Singh, Moirangthem Kiran, Lee, Hane, Merriman, Barry, Jodoin, Jeanne N., Sitaram, Poojitha, Lee, Laura A., Fathalla, Raja, Al-Rawashdeh, Baeth, Ababneh, Osama, El-Khateeb, Mohammad, Escande-Beillard, Nathalie, Nelson, Stanley F., Wu, Yixuan, Tong, Liang, Kenney, Linda J., Roy, Sudipto, Russell, William K., Amiel, Jeanne, Reversade, Bruno, Wagner, Eric J.

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Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number von Hu, Wen F., Pomp, Oz, Ben-Omran, Tawfeg, Kodani, Andrew, Henke, Katrin, Mochida, Ganeshwaran H., Yu, Timothy W., Woodworth, Mollie B., Bonnard, Carine, Raj, Grace Selva, Tan, Thong Teck, Hamamy, Hanan, Masri, Amira, Shboul, Mohammad, Al Saffar, Muna, Partlow, Jennifer N., Al-Dosari, Mohammed, Alazami, Anas, Alowain, Mohammed, Alkuraya, Fowzan S., Reiter, Jeremy F., Harris, Matthew P., Reversade, Bruno, Walsh, Christopher A.

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