Mosaic Turner syndrome: cytogenetics versus FISH von ABULHASAN, S. J., TAYEL, S. M., AL-AWADI, S. A.

Volltext

Deposited Cu (In, Ga) Se2 (CIGS) by spin-coating technique as an absorber layer of solar-cells von Al-Saidi, Sura Salah, Ali, Omar Abdulsada, AL-Awadi, Sarmed S. M.

Volltext

Trisomy 18 in Kuwait von NAGUIB, K. K, AL-AWADI, S. A, MOUSSA, M. A. A, BASTAKI, I, GOUDA, S, REDHA, M. A, MUSTAFA, F, TAYEL, S. M, ABULHASSAN, S. A, MURTHY, D. S. K

Volltext

Kenny-Caffey syndrome: an Arab variant? von Sabry, MA, Farag, TI, Shaltout, AA, Zaki, M, Al-Mazidi, Z, Abulhassan, SJ, Al-Torki, N, Quishawi, A, Al Awadi, SA

Volltext

Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster von Sabry, M A, Zaki, M, Abul Hassan, S J, Ramadan, D G, Abdel Rasool, M A, al Awadi, S A, al Saleh, Q

Volltext

Marinesco-Sjögren syndrome in a Bedouin family von Farah, S., Sabry, M. A., Khuraibet, A. J., Anim, J. T., Quasrawi, B., Al-Khatam, S., Al-Busairi, W., Hussein, J. M., Khan, R. A., Al-Awadi, S. A.

Volltext

A morpho-etiological description of congenital limb anomalies von Tayel, S M, Fawzia, M M, Al-Naqeeb, Niran A, Gouda, Said, Al Awadi, S A, Naguib, K K

Volltext

Triophthalmia and facial clefting: a case report von Tayel, S M, Sabry, M A, Kader, N A, Farah, S, Al-Awadi, S A, Farag, T I

Volltext

High-pressure methanol synthesis case study: safety and environmental impact assessment using consequence analysis von Ahmad, M. A., A. Rashid, Z., El-Harbawi, M., Al-Awadi, A. S.

Volltext

Synaptic, transcriptional and chromatin genes disrupted in autism von De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Ercument Cicek, A., Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas G., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Sean Hill, R., Ionita-Laza, Iuliana, Jimenez Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma’ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Jeremy Willsey, A., Yu, Timothy W., Yuen, Ryan K. C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.

Volltext

Kinetics and mechanism of thermal gas-phase elimination of β-substituted carboxylic acids von Al-Awadi, S.A., Abdallah, M.R., Dib, H.H., Ibrahim, M.R., Al-Awadi, N.A., El-Dusouqui, O.M.E.

Volltext

Familial pericentric inversion of chromosome 1 (p36.3q23) and Bardet-Biedl syndrome von TAYEL, S M, AL-NAGGAR, R L, MURTHY, D S KRISHNA, NAGUIB, K K, AL-AWADI, S A, KARSH, N A ABOU

Volltext

Profile of major congenital malformations in neonates in Al-Jahra region of Kuwait von Madi, S A, Al-Naggar, R L, Al-Awadi, S A, Bastaki, L A

Volltext

The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review von Farag, T I, al-Awadi, S A, Marafie, M J, Bastaki, L, al-Othman, S A, Mohammed, F M, AlSuliman, I S, Murthy, D S

Volltext

Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin baby von Sabry, M A, Obenbergerova, D, Al-Sawan, R, Saleh, Q A, Farah, S, Al-Awadi, S A, Farag, T I

Volltext

Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33) von Al-Awadi, S A, Farag, T I, Naguib, K, Teebi, A, Cuschieri, A, Al-Othman, S, Sundareshan, T S

Volltext

Unusual traits associated with Robinow syndrome von Sabry, M A, Ismail, E A, al-Naggar, R L, al-Torki, N A, Farah, S, al-Awadi, S A, Obenbergerova, D, Bastaki, L

Volltext

Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome von Al-Awadi, S A, Teebi, A S, Farag, T I, Naguib, K M, el-Khalifa, M Y

Volltext

Brachmann-de Lange syndrome in sibs von Naguib, K K, Teebi, A S, Al-Awadi, S A, Marafie, M J

Volltext

Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome? von Al-Awadi, S A, Naguib, K K, Farag, T I, Teebi, A S

Volltext