Hamamy, Hanan: search on Z-Library

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1

Triple A syndrome with a novel indel mutation in the AAAS gene and delayed puberty

Bustanji, Haidar, Sahar, Bashar, Huebner, Angela, Ajlouni, Kamel, Landgraf, Dana, Hamamy, Hanan, Koehler, Katrin

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2015

Language:

english

File:

PDF, 609 KB

english, 2015

2

Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern Iraq

Nasir Al-Allawi, Adil A Eissa, Jaladet MS Jubrael, Shakir AR Jamal, Hanan Hamamy

Journal:

BMC Blood Disorders

Year:

2010

Language:

english

File:

PDF, 590 KB

english, 2010

3

THE CHANGING PROFILE OF CONSANGUINITY RATES IN BAHRAIN, 1990–2009

AL-ARRAYED, SHAIKHA, HAMAMY, HANAN

Journal:

Journal of Biosocial Science

Year:

2012

Language:

english

File:

PDF, 252 KB

english, 2012

4

Clinical and inheritance profiles of Kallmann syndrome in Jordan

Mousa A AbuJbara, Hanan A Hamamy, Nadim S Jarrah, Nadima S Shegem, Kamel M Ajlouni

Journal:

Reproductive Health

Year:

2004

Language:

english

File:

PDF, 672 KB

english, 2004

5

06-P018 Skin development and aging are under the control of the proline metabolic pathway

Nathalie Escande-Beillard, Serene C. Chng, Mohammad Shboul, Hanan Hamamy, Bruno Reversade

Journal:

Mechanisms of Development

Year:

2009

Language:

english

File:

PDF, 46 KB

english, 2009

6

Chromosome aberrations in workers at a tannery in Iraq

Hanan A. Hamamy, Zuhair S. Al-Hakkak, Afaf F. Hussain

Journal:

Mutation Research/Genetic Toxicology

Year:

1987

Language:

english

File:

PDF, 240 KB

english, 1987

7

Familial Monozygotic Twinning: Report of an Extended Multi-generation Family

Hamamy, Hanan A., Ajlouni, Heitham K., Ajlouni, Kamel M.

Journal:

Year:

2004

Language:

english

File:

PDF, 428 KB

english, 2004

8

Is autosomal recessive Silver–Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?

Nadia A. Akawi, Bassam R. Ali, Hanan Hamamy, Azmy Al-Hadidy, Lihadh Al-Gazali

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 11.08 MB

english, 2011

9

Glucose-6-phosphate dehydrogenase deficiency in Iraq

Hanan A. Hamamy, Thanaa Kh. Saeed

Journal:

Year:

1981

Language:

english

File:

PDF, 124 KB

english, 1981

10

Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling

Jing Tian, Ling Ling, Mohammad Shboul, Hane Lee, Brian O'Connor, Barry Merriman, Stanley F. Nelson, Simon Cool, Osama H. Ababneh, Azmy Al-Hadidy, Amira Masri, Hanan Hamamy, Bruno Reversade

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.64 MB

english, 2010

11

Profile of developmental delay in children under five years of age in a highly consanguineous community: A hospital-based study – Jordan

Amira Masri, Hanan Hamamy, Amal Khreisat

Journal:

Brain and Development

Year:

2011

Language:

english

File:

PDF, 111 KB

english, 2011

12

Epidemiological profile of common haemoglobinopathies in Arab countries

Hanan A. Hamamy, Nasir A. S. Al-Allawi

Journal:

Journal of Community Genetics

Year:

2013

Language:

english

File:

PDF, 435 KB

english, 2013

13

Consanguinity and Dysmorphology in Arabs

Al-Gazali, Lihadh, Hamamy, Hanan

Journal:

Year:

2014

Language:

english

File:

PDF, 1.83 MB

english, 2014

14

The ethnic distribution of sickle cell disease in Sudan

Sabahelzain, Majdi Mohammed, Hamamy, Hanan

Journal:

Pan African Medical Journal

Year:

2014

Language:

english

File:

PDF, 380 KB

english, 2014

15

OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

Celine Huber, Mélanie Fradin, Thomas Edouard, Martine Le Merrer, Yasemin Alanay, Daniela Bezerra Da Silva, Albert David, Hanan Hamamy, Liselotte van Hest, Allan M. Lund, Jacques Michaud, Christine Ole

Journal:

Year:

2010

Language:

english

File:

PDF, 274 KB

english, 2010

16

Chromosome aberrations in workers at a storage battery plant in Iraq

Zuhair S. Al-Hakkak, Hanan A. Hamamy, Alya M.B. Murad, Afaf F. Hussain

Journal:

Mutation Research/Genetic Toxicology

Year:

1986

Language:

english

File:

PDF, 490 KB

english, 1986

17

06-P053 ENT3, mutated in H syndrome, is required for proper heart formation

Serene Chng, Mohammad Shboul, Barry Merriman, Laith Akkash, Hanan Hamamy, Bruno Reversade

Journal:

Mechanisms of Development

Year:

2009

Language:

english

File:

PDF, 36 KB

english, 2009

18

Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1

Bonnard, Carine, Strobl, Anna C, Shboul, Mohammad, Lee, Hane, Merriman, Barry, Nelson, Stanley F, Ababneh, Osama H, Uz, Elif, Güran, Tülay, Kayserili, Hülya, Hamamy, Hanan, Reversade, Bruno

Journal:

Nature Genetics

Year:

2012

Language:

english

File:

PDF, 1.06 MB

english, 2012

19

Premarital Screening for Hemoglobinopathies: Experience of a Single Center in Kurdistan, Iraq

Al-Allawi, Nasir A.S., Al-Doski, Adnan A.S., Markous, Raji S.D., Mohamad Amin, Khyria A.K., Eissa, Adil A.Z., Badi, Ameer I.A., Asmaro, Rafal R.H., Hamamy, Hanan

Journal:

Public Health Genomics

Year:

2015

Language:

english

File:

PDF, 467 KB

english, 2015

20

Etiological and clinical profile of neonatal seizures in a highly consanguineous population

Badran, Eman, Masri, Amira, Hamamy, Hanan, Al-Qudah, Abdulkarim

Journal:

Journal of Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 37 KB

english, 2015

21

Consanguinity and reproductive health among Arabs

Ghazi O Tadmouri, Pratibha Nair, Tasneem Obeid, Mahmoud T Al Ali, Najib Al Khaja, Hanan A Hamamy

Journal:

Reproductive Health

Year:

2009

Language:

english

File:

PDF, 583 KB

english, 2009

22

First Report of Clinical, Functional, and Molecular Investigation of Chronic Granulomatous Disease in Nine Jordanian Families

Faris G. Bakri, Cécile Martel, Najwa Khuri-Bulos, Azmi Mahafzah, Mohammad S. El-Khateeb, Adel M. Al-Wahadneh, Wail A. Hayajneh, Hanan A. Hamamy, Elisabeth Maquet, Michelle Molin, Marie José Stasia

Journal:

Journal of Clinical Immunology

Year:

2009

Language:

english

File:

PDF, 623 KB

english, 2009

23

Exome sequencing disclosesKALRNhomozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree

Makrythanasis, Periklis, Guipponi, Michel, Santoni, Federico A., Zaki, Maha, Issa, Mahmoud Y., Ansar, Muhammad, Hamamy, Hanan, Antonarakis, Stylianos E.

Journal:

Year:

2016

Language:

english

File:

PDF, 1.63 MB

english, 2016

24

Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

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

Journal:

Year:

2014

Language:

english

File:

PDF, 6.63 MB

english, 2014

25

Maternal Iron Status in Pregnancy and Long-Term Health Outcomes in the Offspring

Alwan, Nisreen, Hamamy, Hanan

Journal:

Journal of Pediatric Genetics

Year:

2015

Language:

english

File:

PDF, 227 KB

english, 2015

26

Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasia

Gannagé-Yared, Marie-Hélène, Makrythanasis, Periklis, Chouery, Eliane, Sobacchi, Cristina, Mehawej, Cybel, Santoni, Federico A., Guipponi, Michel, Antonarakis, Stylianos E., Hamamy, Hanan, Mégarbané,

Journal:

Year:

2014

Language:

english

File:

PDF, 503 KB

english, 2014

27

Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan

Masri, Amira, Shboul, Mohammad, Khasawneh, Aisha, Jadallah, Rama, ALmustafa, Asma, Escande-Beillard, Nathalie, Hamamy, Hanan, Bakri, Faris, Reversade, Bruno

Journal:

Clinical Neurology and Neurosurgery

Year:

2020

File:

PDF, 2.25 MB

2020

28

06-P029 Congenital hypertelorism & osteopenia, a novel autosomal recessive disease of development

Carine Bonnard, Mohammad Shboul, Nurten Akarsu, Hulya Kayserili, Barry Merriman, Hane Lee, Hanan Hamamy, Bruno Reversade

Journal:

Mechanisms of Development

Year:

2009

Language:

english

File:

PDF, 37 KB

english, 2009

29

Consanguinity and Reproductive Health in Iraq

Hamamy, Hanan A., Al-Hakkak, Zuhair S.

Journal:

Year:

1989

File:

PDF, 574 KB

1989

30

Genomics and Society || The Sociodemographic and Economic Correlates of Consanguineous Marriages in Highly Consanguineous Populations

Year:

2016

Language:

english

File:

PDF, 713 KB

english, 2016

31

Hereditary Multiple Exostoses with Pseudoaneurysm

Azmy M. Al-Hadidy, Moa’ath M. Al-Smady, Azmi A. Haroun, Hanan A. Hamamy, Suha M. Ghoul, Akram O. Shennak

Journal:

CardioVascular and Interventional Radiology

Year:

2007

Language:

english

File:

PDF, 151 KB

english, 2007

32

Rare single gene disorders: estimating baseline prevalence and outcomes worldwide

Blencowe, Hannah, Moorthie, Sowmiya, Petrou, Mary, Hamamy, Hanan, Povey, Sue, Bittles, Alan, Gibbons, Stephen, Darlison, Matthew, Modell, Bernadette

Journal:

Journal of Community Genetics

Year:

2018

Language:

english

File:

PDF, 1022 KB

english, 2018

33

P98. Raiders of the lost FRINGE

Jing Tian, Ling Ling, Mohammad Shboul, Hane Lee, Brian O'Connor, Barry Merriman, Stanley F. Nelson, Simon Cool, Osama H. Ababneh, Azmy Al-Hadidy, Amira Masri, Hanan Hamamy, Bruno Reversade

Journal:

Differentiation

Year:

2010

Language:

english

File:

PDF, 51 KB

english, 2010

34

Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

Temtamy, Samia A., Aglan, Mona S., Otaify, Ghada A., Abdel-Hamid, Mohamed, Ismail, Somaia, Makrythanasis, Periklis, Hamamy, Hanan, Antonarakis, Stylianos E.

Journal:

Middle East Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 435 KB

english, 2015

35

Canavan disease: A first case from Jordan

Masri, Amira, Hamamy, Hanan

Journal:

Journal of Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 68 KB

english, 2015

36

Male transient hip osteoporosis: are physicians at a higher risk?

Azmy M. Hadidy, Nosaiba T. Al Ryalat, Shaher T. Hadidi, Emad S. Tarawneh, Maher T. Hadidi, Osama A. Samara, Deema M. Abu-Labn, Lawrence M. Al-Rousan, Dana A. Hiyasat, Hanan A. Hamamy

Journal:

Archives of Osteoporosis

Year:

2009

Language:

english

File:

PDF, 139 KB

english, 2009

37

Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders

Deiana, Manila, Herrero, Carmen Roche, Zampino, Giuseppe, Hamamy, Hanan, Zalloum, Yusra, Waaler, Per Erik, Meloni, Alessandra, Marongiu, Mara, Chiappe, Francesca, Herholz, Jana

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 1.06 MB

english, 2011

38

ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia

Shammas, Christos, Papasavva, Thessalia, Felekis, Xenia, Christophorou, Christos, Roomere, Hanno, Synodinos, Jan Traeger, Kanavakis, Emmanuel, El-Khateeb, Mohammed, Hamamy, Hanan, Mahmoud, Tamara, Shb

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2010

Language:

english

File:

PDF, 196 KB

english, 2010

39

Sickle Cell Disease in the Kurdish Population of Northern Iraq

Al-Allawi, Nasir A.S., Jalal, Sana D., Nerwey, Farida F., Al-Sayan, Galawezh O.O., Al-Zebari, Sahima S.M., Alshingaly, Awny A., Markous, Raji D., Jubrael, Jaladet M.S., Hamamy, Hanan

Journal:

Year:

2012

Language:

english

File:

PDF, 251 KB

english, 2012

40

A Novel Homozygous Mutation in FGFR3 Causes Tall Stature, Severe Lateral Tibial Deviation, Scoliosis, Hearing Impairment, Camptodactyly, and Arachnodactyly

Makrythanasis, Periklis, Temtamy, Samia, Aglan, Mona S., Otaify, Ghada A., Hamamy, Hanan, Antonarakis, Stylianos E.

Journal:

Year:

2014

Language:

english

File:

PDF, 811 KB

english, 2014

41

Epidemiological profile of neural tube defects in Arab countries

Journal:

Middle East Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 590 KB

english, 2014

42

Familial epilepsy in Algeria: Clinical features and inheritance profiles

Chentouf, Amina, Dahdouh, Aïcha, Guipponi, Michel, Oubaiche, Mohand Laïd, Chaouch, Malika, Hamamy, Hanan, Antonarakis, Stylianos E.

Journal:

Year:

2015

Language:

english

File:

PDF, 117 KB

english, 2015

43

Communities and community genetics in Ethiopia

Tadesse, Luche, Tafesse, Fikru, Hamamy, Hanan

Journal:

Pan African Medical Journal

Year:

2014

Language:

english

File:

PDF, 446 KB

english, 2014

44

Parental decisions following the prenatal diagnosis of sex chromosome abnormalities

Hanan A Hamamy, Sophie Dahoun

Journal:

European Journal of Obstetrics & Gynecology and Reproductive Biology

Year:

2004

Language:

english

File:

PDF, 93 KB

english, 2004

45

06-P037 Dubowitz syndrome maps to chromosome 12 within an interval of 70 genes

Jing Tian, Mohammad Shboul, Barry Merriman, Hane Lee, Hanan Hamamy, Bruno Reversade

Journal:

Mechanisms of Development

Year:

2009

Language:

english

File:

PDF, 48 KB

english, 2009

46

Jordan: Communities and Community Genetics

Hamamy, Hanan, Al-Hait, Sana, Alwan, Aladin, Ajlouni, Kamel

Journal:

Community Genetics

Year:

2007

Language:

english

File:

PDF, 199 KB

english, 2007

47

Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction

Al Sayed, Zeina R, Canac, Robin, Cimarosti, Bastien, Bonnard, Carine, Gourraud, Jean-Baptiste, Hamamy, Hanan, Kayserili, Hulya, Girardeau, Aurore, Jouni, Mariam, Jacob, Nicolas, Gaignerie, Anne, Chari

Journal:

Cardiovascular Research

Year:

2020

File:

PDF, 1.62 MB

2020

48

Familial Monozygotic Twinning: Report of an Extended Multi-generation Family

Hamamy, Hanan A., Ajlouni, Heitham K., Ajlouni, Kamel M.

Journal:

Year:

2004

Language:

english

File:

PDF, 283 KB

english, 2004

49

Community genetics. Its definition 2010

Leo P. ten Kate, Lihadh Al-Gazali, Sonia Anand, Alan Bittles, Jean-Jacques Cassiman, Arnold Christianson, Martina C. Cornel, Hanan Hamamy, Helena Kääriäinen, Ulf Kristoffersson, David Marais, Victor B

Journal:

Journal of Community Genetics

Year:

2010

Language:

english

File:

PDF, 89 KB

english, 2010

50

P106. Congenital hypertelorism and osteopenia: A novel autosomal recessive disease

Carine Bonnard, Barry Merriman, Hane Lee, Hülya Kayserili, Nurten Akarsu, Anna Strobl, Mohammad Shboul, Hanan Hamamy, Bruno Reversade

Journal:

Differentiation

Year:

2010

Language:

english

File:

PDF, 47 KB

english, 2010

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