L. Hilal

发表

Genotype-Phenotype Correlation in Moroccan Patients With Primary Congenital Glaucoma

F. Gaboun, A. Berraho, A. Serrou, 2015, Journal of glaucoma.

A homozygous insertion–deletion in the type VII collagen gene (COL7A1) in Hallopeau–Siemens dystrophic epidermolysis bullosa

Y. Barrandon, J. Uitto, A. Christiano, 1993, Nature Genetics.

Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature

Y. Bakri, M. Khattab, L. Hessissen, 2018, Clinical lymphoma, myeloma & leukemia.

Molecular analysis of the rearranged during transfection proto-oncogene in Moroccan patients with medullary thyroid carcinoma

Y. Bakri, A. Chraibi, M. El Mzibri, 2015 .

Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosa.

J. Uitto, A. Christiano, A. Hovnanian, 1994, American journal of human genetics.

A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex

Y. Barrandon, A. Hovnanian, M. Goossens, 1993, Nature Genetics.

Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosa.

M Goossens, J. Uitto, A. Christiano, 1994, American journal of human genetics.

DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrence.

J. Terwilliger, C. Bodemer, A. Christiano, 1995, The Journal of investigative dermatology.

Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature.

J. Pantel, S. Amselem, Y. Le Bouc, 2006, The Journal of clinical investigation.

Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: Three novel mutations in CYP1B1

M. El Mzibri, A. Berraho, A. Serrou, 2010, Molecular vision.

Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts

O. Gribouval, A. Basak, M. Abitbol, 2003, Journal of medical genetics.

Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism

J. Pantel, S. Amselem, N. Collot, 2015, Clinical endocrinology.

Unusual Phenotypic Features in a Patient with a Novel Splice Mutation in the GHRHR Gene

S. Amselem, M. Sobrier, A. Kadiri, 2008, Molecular medicine.

Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts

O. Gribouval, J. Dufier, M. Abitbol, 2002, Ophthalmic genetics.

[C634R mutation of the protooncongene RET and molecular diagnosis in multiple endocrine neoplasia type 2 in a large Moroccan family].

A. Kadiri, A. Chraibi, L. Hilal, 2008, Bulletin du Cancer.

[Characterization of RET proto-oncogene C634Y mutation in a Moroccan family with multiple endocrine neoplasia type 2A].

A. Kadiri, L. Hilal, B. Benazzouz, 2006, Annales d'Endocrinologie.

20-Hydroxyecdysone regulates cytoplasmic actin gene expression in Drosophila cultured cells.

B. Dastugue, J. Couderc, M. Sobrier, 1987, Nucleic acids research.

Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism

J. Pantel, S. Amselem, N. Collot, 2015, Clinical endocrinology.