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1

Another case of the human homologue of the mouse mutant disorganization

Ahmad S. Teebi, Alison M. Elliott

Journal:

American Journal of Medical Genetics Part A

Year:

1996

Language:

english

File:

PDF, 119 KB

english, 1996

2

Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis in three related children and the association with Sweet syndrome in two siblings

H.A. Majeed, Malak Kalaawi, D. Mohanty, A.S. Teebi, M.F. Tunjekar, F. Al-Gharbawy, S.A. Majeed, A.H. Al-Gazzar

Journal:

The Journal of Pediatrics

Year:

1989

Language:

english

File:

PDF, 1.93 MB

english, 1989

3

Pseudo-trisomy 13 syndrome with upper limb shortness and radial hypoplasia

Richard G. Boles, Ahmad S. Teebi, Kathryn A. Neilson, M. Stephen Meyn

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 315 KB

english, 1992

4

Uncle-niece / aunt-nephew marriages are not existing in Muslim Arabs

Ahmad S. Teebi, Makia J. Marafie

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 49 KB

english, 1988

5

Alagille syndrome with de Novo del(20) (p 11.2)

Dr. Ahmad S. Teebi, D. S. Krishna Murthy, E. A. R. Ismail, A. A. Redha

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 272 KB

english, 1992

6

Nablus mask-like facial syndrome

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 103 KB

english, 2000

7

Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia

Muhammad Faiyaz-Ul-Haque, Wasim Ahmad, Abdul Wahab, Sayedul Haque, Anser C. Azim, Syed H.E. Zaidi, Ahmad S. Teebi, Mahmud Ahmad, Daniel H. Cohn, Teepu Siddique, Lap-Chee Tsui

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 243 KB

english, 2002

8

Nonsyndromal anencephaly: Possible autosomal recessive variant

Talaat I. Farag, Ahmad S. Teebi, Dr. Sadika A. Al-Awadi, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 306 KB

english, 1986

9

Autosomal dominant idiopathic scoliosis?

Morag Bell, Dr. Ahmad S. Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 83 KB

english, 1995

10

Trigonomicrocephaly, severe micrognathia, large ears, atrioventricular septal defect, symmetrical cutaneous syndactyly of hands and feet, and multiple café-au-lait spots: New acrocraniofacial dysostosis syndrome?

Nouriya Al-Sannaa, C.R. Forrest, Ahmad S. Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 248 KB

english, 2001

11

Newly recognized autosomal recessive acrofacial dysostosis syndrome resembling Nager syndrome

Shelley J. Kennedy, Ahmad S. Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 216 KB

english, 2004

12

Primary hypomagnesaemia

K. I. Dudin, A. S. Teebi

Journal:

European Journal of Pediatrics

Year:

1987

Language:

english

File:

PDF, 383 KB

english, 1987

13

New autosomal dominant syndrome reminiscent of Coffin-Siris syndrome and Brachymorphism-Onychodysplasia-Dysphalangism syndrome

Elliott, Alison M., Teebi, Ahmad S.

Journal:

Clinical Dysmorphology

Year:

2000

File:

PDF, 1.93 MB

2000

14

Population and molecular genetic update: the second Middle East Genetics Association of America (MEGA) conference

Teebi, Ahmad S., Shawky, Rabah M.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 62 KB

english, 2000

15

Further examples of autosomal dominant transmission of nonsyndromic aplasia cutis congenita

Elliott, Alison M., Teebi, Ahmad S.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 23 KB

english, 1997

16

Detecting rearrangements in children using subtelomeric FISH and SKY

Blaise Clarkson, Katerina Pavenski, Lucie Dupuis, Shelley Kennedy, Stephen Meyn, Marjan M. Nezarati, Gloria Nie, Rosanna Weksberg, Stephen Withers, Nada Quercia, Ahmad S. Teebi, Ikuko Teshima

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 477 KB

english, 2002

17

Further delineation of the Van den Ende–Gupta syndrome

Rehab Ali, Mariam Almureikhi, Fatima Al-Musaifri, Venkatraman Bhat, Ahmad Teebi, Tawfeg Ben-Omran

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 296 KB

english, 2010

18

Velo-facio-skeletal syndrome in a mother and daughter

Dr. Ahmad S. Teebi, Mazin B. Qumsiyeh, Cynthia H. Meyers-Seifer, M. Stephen Meyn

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 439 KB

english, 1995

19

Arab genetic disease database (AGDDB): A population-specific clinical and mutation database

Ahmad S. Teebi, Saeed A. Teebi, Christopher J. Porter, A. Jamie Cuticchia

Journal:

Year:

2002

Language:

english

File:

PDF, 529 KB

english, 2002

20

Alopecia congenita universalis, microcephaly, cutis marmorata, short stature and XY gonadal dysgenesis: variable expression of El-Shanti syndrome

AhmadS. Teebi, Lucie Dupuis, Diane Wherrett, Anthony Khoury, KennethJ. Zucker

Journal:

European Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 165 KB

english, 2004

21

Genetic Disorders Among Arab Populations || Familial Mediterranean Fever and Other Autoinflammatory Disorders

Teebi, Ahmad S.

Year:

2010

Language:

english

File:

PDF, 422 KB

english, 2010

22

Monozygotic Twins Concordant for Bardet-Biedl Syndrome and Benign Acanthosis nigricans

Farag, T.I., Teebi, A.S., Al-Awadi, S.A., El-Ramly, M.A.

Journal:

Medical Principles and Practice

Year:

1989

File:

PDF, 400 KB

1989

23

Not a new Seckel-like syndrome but ear-patella-short stature syndrome

Teebi, Ahmad S., Gorlin, Robert J.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 83 KB

english, 1997

24

Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification

Andrea C. Stachon, Berivan Baskin, Adam C. Smith, Andrea Shugar, Cheryl Cytrynbaum, Leona Fishman, Roberto Mendoza-Londono, Regan Klatt, Ahmed Teebi, Peter N. Ray, Rosanna Weksberg

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 258 KB

english, 2007

25

A new autosomal recessive disorder resembling Weaver syndrome

Dr. Ahmad S. Teebi, T. S. Sundareshan, Mousa Y. Hammouri, Sadika A. Al-Awadi, Qasem A. Al-Saleh

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 385 KB

english, 1989

26

A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type

Muhammad Faiyaz-Ul-Haque, Syed Hassan Ejaz Zaidi, Mariam Al-Ali, Mariam S. Al-Mureikhi, Shelley Kennedy, Ghalia Al-Thani, Lap-Chee Tsui, Ahmad Said Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 305 KB

english, 2004

27

Developmental anomalies suggestive of the human homologue of the mouse mutant disorganization

Alison M. Elliott, Moy-Fong Chen, E. Michel Azouz, Dr. Ahmad S. Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 381 KB

english, 1995

28

Siblings with a progressive neurodegenerative condition associated with basal ganglia calcifications, retinitis pigmentosa and decreased levels of fucosidase — a new presentation?

S. Portoian-Shuhaiber, K. Gumaa, H. Hamalawi, O. K. Malla, A. S. Teebi, A. Al-Rashied

Journal:

Journal of Inherited Metabolic Disease

Year:

1987

Language:

english

File:

PDF, 156 KB

english, 1987

29

Letter to the Editors : The second family with Spahr-type metaphyseal chondrodysplasia: autosomal recessive inheritance confirmed

Talaat I. Farag, Ahmad S. Teebi

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 232 KB

english, 1990

30

Not a new variant of the autosomal recessive multiple pterygium syndrome but the Bartsocas-Papas syndrome

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 32 KB

english, 2001

31

Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?

Talaat I. Farag, Dr. Ahmad S. Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 260 KB

english, 1990

32

Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 gene

SHE Zaidi, S Meyer, I Peltekova, AS Teebi, M Faiyaz-Ul-Haque

Journal:

Clinical Genetics

Year:

2009

Language:

english

File:

PDF, 59 KB

english, 2009

33

Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families

M Faiyaz-Ul-Haque, SHE Zaidi, AA Wahab, A Eltohami, MS Al-Mureikhi, G Al-Thani, VD Peltekova, L-C Tsui, AS Teebi

Journal:

Clinical Genetics

Year:

2008

Language:

english

File:

PDF, 545 KB

english, 2008

34

New autosomal recessive faciodigitogenital syndrome.

Teebi, A S, Naguib, K K, Al-Awadi, S, Al-Saleh, Q A

Journal:

Journal of Medical Genetics

Year:

1988

Language:

english

File:

PDF, 1.74 MB

english, 1988

35

The Prevalence of Attention Deficit Hyperactivity Symptoms in Schoolchildren in a Highly Consanguineous Community

Bener, Abdulbari, Al Qahtani, Razna, Teebi, Ahmad S., Bessisso, Mohammed

Journal:

Medical Principles and Practice

Year:

2008

Language:

english

File:

PDF, 126 KB

english, 2008

36

Inherited duplication, dup (8) (p23.1p23.1) pat, in a father and daughter with congenital heart defects

Shelley J. Kennedy, Ahmad S. Teebi, Ian Adatia, Ikuko Teshima

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 57 KB

english, 2001

37

Teebi hypertelorism syndrome: Report of a family with previously unrecognized findings

Anne Chun-Hui Tsai, Jacqualyn R. Robertson, Ahmad S. Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 142 KB

english, 2002

38

Brachmann-de Lange syndrome in sibs.

Naguib, K K, Teebi, A S, Al-Awadi, S A, Marafie, M J

Journal:

Journal of Medical Genetics

Year:

1987

Language:

english

File:

PDF, 601 KB

english, 1987

39

Book review

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 26 KB

english, 2004

40

Phenotypic heterogeneity in Woodhouse–Sakati syndrome: Two new families with a mutation in the C2orf37 gene

Tawfeg Ben-Omran, Rehab Ali, Mariam Almureikhi, Seham Alameer, Muna Al-Saffar, Christopher A. Walsh, Jillian M. Felie, Ahmad Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 160 KB

english, 2011

41

Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

M Faiyaz-Ul-Haque, W Ahmad, SHE Zaidi, S Haque, AS Teebi, M Ahmad, DH Cohn, L-C Tsui

Journal:

Clinical Genetics

Year:

2002

Language:

english

File:

PDF, 67 KB

english, 2002

42

A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome

Muhammad Faiyaz-Ul-Haque, Syed H.E. Zaidi, Nouriyah Al-Sanna, Abdulrahman Alswaid, Tariq Momenah, Namik Kaya, Fouad Al-Dayel, Issam Bouhoaigah, Mohammed Saliem, Lap-Chee Tsui, Ahmad S. Teebi

Journal:

Atherosclerosis

Year:

2009

Language:

english

File:

PDF, 921 KB

english, 2009

43

Prenatal diagnosis of fragile X syndrome: identification of a male fetus mosaic for a premutation on chorionic villus sampling - management and follow-up

Kennedy, S J, Wei, C, Steele, L, Teebi, A S

Journal:

Genetics in Medicine

Year:

2000

Language:

english

File:

PDF, 126 KB

english, 2000

44

Keutel syndrome: Further characterization and review

Teebi, Ahmad S., Lambert, Deborah M., Kaye, Glenn M., Al-Fifi, Sulaiman, Tewfik, Ted L., Azouz, E. Michel

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 453 KB

english, 1998

45

Down syndrome in Kuwait

S. A. Al-Awadi, T. I. Farag, A. S. Teebi, K. K. Naguib, T. S. Sundareshan, Dr. D. S. Krishna Murthy

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 238 KB

english, 1990

46

Reply to Ruiter et al.: A possible example of acrofacial dysostosis type Kennedy–Teebi

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 24 KB

english, 2005

47

De novopartial monosomy 21 with unusual karyotype

S. A. Al-Awadi, K. K. Naguib, A. S. Teebi, T. S. Sundareshan

Journal:

Journal of Human Genetics

Year:

1986

Language:

english

File:

PDF, 451 KB

english, 1986

48

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

Kantarci, Sibel, Al-Gazali, Lihadh, Hill, R Sean, Donnai, Dian, Black, Graeme C M, Bieth, Eric, Chassaing, Nicolas, Lacombe, Didier, Devriendt, Koen, Teebi, Ahmad

Journal:

Nature Genetics

Year:

2007

Language:

english

File:

PDF, 236 KB

english, 2007

49

Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardation

D. S. Krishna Murthy, A. S. Teebi, T. S. Sundareshan, S. A. Al-Awadi

Journal:

Indian Journal of Pediatrics

Year:

1990

Language:

english

File:

PDF, 220 KB

english, 1990

50

Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome

Natascia Anastasio, Tawfeg Ben-Omran, Ahmad Teebi, Kevin C.H. Ha, Emilie Lalonde, Rehab Ali, Mariam Almureikhi, Vazken M. Der Kaloustian, Junhui Liu, David S. Rosenblatt, Jacek Majewski, Loydie A. Jer

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 639 KB

english, 2010

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