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Analyse génétique du syndrome de Turner : étude tunisienne de 89 cas

Annales d'endocrinologie, 2008, Vol.69 (5), p.440-445

2008

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Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V

Clinical genetics, 2010-10, Vol.78 (4), p.398-401

2010

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Performance limitations in the robust servomechanism problem for discrete-time LTI systems

IEEE transactions on automatic control, 2003-08, Vol.48 (8), p.1299-1311

2003

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Role of new generation sequencing in the diagnosis of intractable diarrhea

Clinica chimica acta, 2024-05, Vol.558, p.118281, Article 118281

2024

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The arthrogryposis - renal dysfunction - cholestasis syndrome: A case report

Clinica chimica acta, 2024-05, Vol.558, p.118282, Article 118282

2024

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Progressive familial intrahepatic cholestasis type 3 or neonatal sclerosing cholangitis? about four Tunisian families

Clinica chimica acta, 2024-05, Vol.558, p.118283, Article 118283

2024

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Genetic analysis of Turner syndrome: 89 cases in Tunisia

Annales d'endocrinologie, 2008-11, Vol.69 (5), p.440-445

2008

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Y chromosome microdeletions in Tunisian infertile males

Pathologie biologie (Paris), 2008-05, Vol.56 (3), p.111-115

2008

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Analyse génétique du syndrome de Tumer : étude tunisienne de 89 cas

Annales d'endocrinologie, 2008, Vol.69 (5), p.440-445

2008

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Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation

The journal of clinical endocrinology and metabolism, 2004-01, Vol.89 (1), p.368-374

2004

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MEFV Mutations in Tunisian Patients Suffering from Familial Mediterranean Fever

Seminars in arthritis and rheumatism, 2007-06, Vol.36 (6), p.397-401

2007

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Performance limitations in the robust servomechanism problem for discrete time periodic systems

Automatica (Oxford), 2003-06, Vol.39 (6), p.1053-1059

2003

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Only two mutations detected in 15 Tunisian patients with 11[beta]-hydroxylase deficiency: the p.Q356X and the novel p.G379V

Clinical genetics, 2010-10, Vol.78 (4), p.398

2010

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Only two mutations detected in 15 Tunisian patients with 11b-hydroxylase deficiency: the p.Q356X and the novel p.G379V

Clinical genetics, 2010-10, Vol.78 (4), p.398-401

2010

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Limiting performance of optimal linear discrete filters

Automatica (Oxford), 2003-07, Vol.39 (7), p.1221-1226

2003

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Epidemiologic and genetic study of trisomy 21 in Tunisia

Tunisie Medicale, 1999-08, Vol.77 (8-9), p.407

1999

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Value and practical applications of cytogenetic in situ hybridization technique

Tunisie Medicale, 1998-05, Vol.76 (5), p.113

1998

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Cytogenetic study of 500 patients selected in the research for chromosomal anomalies

Tunisie Medicale, 1992-01, Vol.70 (1), p.39

1992

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Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family

Clinical dysmorphology, 2005-01, Vol.14 (1), p.23-25

2005

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Molecular studies of chromosome Y in 20 patients with 46,XY karyotype

Tunisie Medicale, 1997-10, Vol.75 (10), p.762

1997

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Syndrome of ocular, skeletal & abdominal abnormalities

Genetics in medicine, 2000-01, Vol.2 (1), p.83

2000

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Genetic study of two Tunisian Ehlers Danlos syndrome type VI

Genetics in medicine, 2000-01, Vol.2 (1), p.83

2000

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The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain

Comparative and functional genomics, 2008-01, Vol.2008 (2008), p.1-5

2008

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PERFORMANCE LIMITATIONS IN THE RIPPLE-FREE ROBUST SERVOMECHANISM PROBLEM FOR SAMPLED LTI SYSTEMS

IFAC Proceedings Volumes, 2002, Vol.35 (1), p.467-472

2002

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Performance limitations in the robust servomechanism problem for proper sampled LTI systems

IFAC Proceedings Volumes, 2000-07, Vol.33 (20), p.13-18

2000

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Analyse génétique du syndrome de Turner : étude tunisienne de 89 cas

Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V

Performance limitations in the robust servomechanism problem for discrete-time LTI systems

Role of new generation sequencing in the diagnosis of intractable diarrhea

The arthrogryposis - renal dysfunction - cholestasis syndrome: A case report

Progressive familial intrahepatic cholestasis type 3 or neonatal sclerosing cholangitis? about four Tunisian families

Genetic analysis of Turner syndrome: 89 cases in Tunisia

Y chromosome microdeletions in Tunisian infertile males

Analyse génétique du syndrome de Tumer : étude tunisienne de 89 cas

Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation

MEFV Mutations in Tunisian Patients Suffering from Familial Mediterranean Fever

Performance limitations in the robust servomechanism problem for discrete time periodic systems

Only two mutations detected in 15 Tunisian patients with 11[beta]-hydroxylase deficiency: the p.Q356X and the novel p.G379V

Only two mutations detected in 15 Tunisian patients with 11b-hydroxylase deficiency: the p.Q356X and the novel p.G379V

Limiting performance of optimal linear discrete filters

Epidemiologic and genetic study of trisomy 21 in Tunisia

Value and practical applications of cytogenetic in situ hybridization technique

Cytogenetic study of 500 patients selected in the research for chromosomal anomalies

Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family

Molecular studies of chromosome Y in 20 patients with 46,XY karyotype

Syndrome of ocular, skeletal & abdominal abnormalities

Genetic study of two Tunisian Ehlers Danlos syndrome type VI

The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain

PERFORMANCE LIMITATIONS IN THE RIPPLE-FREE ROBUST SERVOMECHANISM PROBLEM FOR SAMPLED LTI SYSTEMS

Performance limitations in the robust servomechanism problem for proper sampled LTI systems

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