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Prevalence of Behçet's disease in an Arab community in Israel

Annals of the rheumatic diseases, 2002-04, Vol.61 (4), p.365-366

2002

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Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

European journal of human genetics : EJHG, 1999-04, Vol.7 (3), p.287-292

1999

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Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups

European journal of human genetics : EJHG, 2000-04, Vol.8 (4), p.307-310

2000

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Trends in the frequencies of consanguineous marriages in the Israeli Arab community

Clinical genetics, 2000-08, Vol.58 (2), p.106-110

2000

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Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis

Pediatrics (Evanston), 2000-05, Vol.105 (5), p.E70-e70

2000

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Facial clefting in an Arab town in Israel

Clinical genetics, 2002-06, Vol.61 (6), p.448-453

2002

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Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel

American journal of human genetics, 2001-08, Vol.69 (2), p.351-360

2001

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Familial Mediterranean fever—A review

Genetics in medicine, 2011-06, Vol.13 (6), p.487-498

2011

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A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11

Clinical genetics, 2005-08, Vol.68 (2), p.185-187

2005

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Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab women

The Israel Medical Association journal, 2000-05, Vol.2 (5), p.346-350

2000

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Pathological fractures in spondyloenchondrodysplasia : case report

Pediatric radiology, 2000-02, Vol.30 (2), p.119-120

2000

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Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies

The Israel Medical Association journal, 2001-07, Vol.3 (7), p.488-491

2001

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Supramicron-sized particle clearance from alveoli: route and kinetics

Journal of applied physiology (1985), 1990-10, Vol.69 (4), p.1302-1308

1990

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Determining deposition sites of inhaled lung particles and their effect on clearance

Journal of applied physiology (1985), 1990-04, Vol.68 (4), p.1427-1434

1990

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Myotonic dystrophy-no evidence for preferential transmission of the mutated allele: A prenatal analysis

American journal of medical genetics. Part A, 2004-05, Vol.127A (1), p.50-53

2004

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Patient's perceptions of an anesthesia preoperative computerized patient interview

Journal of clinical monitoring and computing, 1999-12, Vol.15 (7-8), p.503-507

1999

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Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G

American journal of otolaryngology, 1999, Vol.20 (1), p.64-67

1999

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The Security Circuit: A Proposed Construct for the Central Nervous System

International journal of neuroscience, 2000-01, Vol.102 (1-4), p.1-254

2000

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Demographic characteristics of the Israeli Arab community in connection with consanguinity

Israel journal of medical sciences, 1996-12, Vol.32 (12), p.1286

1996

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Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24

Annales de génétique, 1996, Vol.39 (3), p.181

1996

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Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes

American journal of medical genetics, 2000-07, Vol.93 (2), p.155-157

2000

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Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation

American journal of medical genetics, 1998-12, Vol.80 (5), p.526-528

1998

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Solar activity cycle and the incidence of foetal chromosome abnormalities detected at prenatal diagnosis

International journal of biometeorology, 1995-11, Vol.39 (2), p.59-63

1995

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Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter

American journal of medical genetics, 2001-11, Vol.104 (2), p.152-156

2001

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Agenesis of the corpus callosum in a mother and son

American journal of medical genetics, 1997-03, Vol.69 (2), p.152-154

1997

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Prevalence of Behçet's disease in an Arab community in Israel

Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups

Trends in the frequencies of consanguineous marriages in the Israeli Arab community

Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis

Facial clefting in an Arab town in Israel

Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel

Familial Mediterranean fever—A review

A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11

Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab women

Pathological fractures in spondyloenchondrodysplasia : case report

Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies

Supramicron-sized particle clearance from alveoli: route and kinetics

Determining deposition sites of inhaled lung particles and their effect on clearance

Myotonic dystrophy-no evidence for preferential transmission of the mutated allele: A prenatal analysis

Patient's perceptions of an anesthesia preoperative computerized patient interview

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G

The Security Circuit: A Proposed Construct for the Central Nervous System

Demographic characteristics of the Israeli Arab community in connection with consanguinity

Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24

Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes

Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation

Solar activity cycle and the incidence of foetal chromosome abnormalities detected at prenatal diagnosis

Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter

Agenesis of the corpus callosum in a mother and son

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