Bastaki, Laila: search on Z-Library

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1

Quand tous les chemins mènent à l’Afrique…

Urtizberea, J. Andoni, Alrohaif, Hadil, Gouda, Sayed A., Bastaki, Laila

Journal:

médecine/sciences

Year:

2019

Language:

french

File:

PDF, 6.20 MB

french, 2019

2

Clustering of cri du chat syndrome among the Bedouins

Dr. Talaat I. Farag, Sadika A. Al-Awadi, Makia J. Marafie, Laila Bastaki, D. S. Krishna Murthy, Sulaiman A. Al-Othman, Fawziyah M. Mohamed, Amira A. Reda, Sawsan J. Abul Hasan, Mariam A. Reda, Lulwa A

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 180 KB

english, 1993

3

Woodhouse–Sakati syndrome in six Kuwaiti families

Bastaki, Laila, Al-Wadaani, Amal, Gouda, Sayed, Al-Aboud, Hayat, Elshafey, Alaa

Journal:

Middle East Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 366 KB

english, 2013

4

Pallister–Killian syndrome with fibular hypoplasia

Sadik, Doaa I., Al-Hathal, Muneef, Ghareeb, Tarek M., Abulhasan, Sawsan J., Bastaki, Laila A.

Journal:

Middle East Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 169 KB

english, 2016

5

Quand tous les chemins mènent à l’Afrique…

Urtizberea, J. Andoni, Alrohaif, Hadil, Gouda, Sayed A., Bastaki, Laila

Journal:

médecine/sciences

Year:

2019

File:

PDF, 6.20 MB

2019

6

CTG Repeat Number at the Myotonic Dystrophy Locus in Healthy Kuwaiti Individuals

Alfadhli, Suad, Elshafey, Alaa E., Bastaki, Lailá, Al-Awadi, Sadeqa

Journal:

Archives of Neurology

Year:

2004

Language:

english

File:

PDF, 91 KB

english, 2004

7

GNE myopathy in the Bedouin population of Kuwait: Genetics, prevalence and clinical description

Alrohaif, Hadil, Pogoryelove, Oksana, Al-Ajmi, Abdullah, Aljeryan, Lulwa A, Alrashidi, Nuwayer H, Alefasi, Sara A, Urtizberea, Andoni, Lochmüller, Hanns, Bastaki, Laila

Journal:

Year:

2018

Language:

english

File:

PDF, 1.30 MB

english, 2018

8

Autosomal recessive Congenital Diaphragmatic Defects in the Arabs

Talaat I. Farag, Laila Bastaki, Makia Marafie, Sadika A. Al-Awadi, Judith Krsz

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 194 KB

english, 1994

9

Recurrent homozygous damaging mutation in TMX2 , encoding a protein disulfide isomerase, in four families with microlissencephaly

Ghosh, Shereen Georges, Wang, Lu, Breuss, Martin W, Green, Joshua D, Stanley, Valentina, Yang, Xiaoxu, Ross, Danica, Traynor, Bryan J, Alhashem, Amal M, Azam, Matloob, Selim, Laila, Bastaki, Laila, El

Journal:

Journal of Medical Genetics

Year:

2020

Language:

english

File:

PDF, 1.15 MB

english, 2020

10

Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine

Mohammed, Fawziah, Elshafey, Alaa, Al-balool, Haya, Alaboud, Hayat, Al Ben Ali, Mohammed, Baqer, Adel, Bastaki, Laila, Al-Aama, Jumana Yousuf

Journal:

Year:

2018

Language:

english

File:

PDF, 1.66 MB

english, 2018

11

Novel STAMBP mutation and additional findings in an Arabic family

Faqeih, Eissa A., Bastaki, Laila, Rosti, Rasim Ozgur, Spencer, Emily G., Zada, AbdulAli P., Saleh, Mohammad A. M., Um, Kyongmi, Gleeson, Joseph G.

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 559 KB

english, 2015

12

A case report of FATCO syndrome

Bastaki, Laila A., Al-Hathal, Muneef, Sadik, Doaa I., Alrohaif, Hadil E., Yousef, Hala Y., Khallaf, Mohamed G.

Journal:

Middle East Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 209 KB

english, 2015

13

Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia

Akizu, Naiara, Shembesh, Nuri M., Ben-Omran, Tawfeg, Bastaki, Laila, Al-Tawari, Asma, Zaki, Maha S., Koul, Roshan, Spencer, Emily, Rosti, Rasim Ozgur, Scott, Eric, Nickerson, Elizabeth, Gabriel, Stace

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 954 KB

english, 2013

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