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Antenatal diagnosis of tuberous sclerosis

The Lancet (British edition), 1993-01, Vol.341 (8838), p.176

1993

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Increased chromosomal breakage in epileptic children after long-term treatment

European journal of pediatrics, 1986-10, Vol.145 (5), p.439-442

1986

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Mating between two balanced translocation carriers in two unrelated families

Human genetics, 1983-12, Vol.65 (2), p.165-168

1983

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Antenatal diagnosis of tuberous sclerosis

The Lancet (British edition), 1993-01, Vol.341 (8838), p.176-177

1993

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Prenatal diagnosis of deletion 11q23-->qter. Report of two unrelated cases

Annales de génétique, 1993, Vol.36 (4), p.228

1993

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Identification of the origin of a 22p+ chromosome by triplex dosage effect of LDH B, GAPHD, TPI and ENO2

Annales de génétique, 1980, Vol.23 (2), p.111

1980

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Infantile Spasms and the CHARGE Association

Developmental medicine and child neurology, 1983-06, Vol.25 (3), p.367-369

1983

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t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome

Annales de génétique, 1982, Vol.25 (1), p.56

1982

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Mosaicism 45,X/46,X,r/(Y) associated with mixed gonadal dysgenesis. Description of a case and review of the literature

La Pediatria medica e chirurgica, 1987-07, Vol.9 (4), p.495

1987

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Fanconi's anemia type Estren-Dameshek. A case report (author's transl)

La Pediatria medica e chirurgica, 1981-11, Vol.3 (6), p.575

1981

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Ultrastructural and Biological Characterization of Human Choroid Cell Cultures Transformed by Simian Virus 40

In Vitro, 1983-06, Vol.19 (6), p.443-452

1983

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Biological and ultrastructural characteristics of a line of human choroid transformed by SV40

Annali dell'Istituto superiore di sanità, 1982, Vol.18 (3), p.379-384

1982

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Variability of r(22) chromosomes phenotypical expression

Acta geneticae medicae et gemellologiae, 1977, Vol.26 (3-4), p.287

1977

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2 new cases of chromosome 22 with ring structure

Pathologica, 1979-05, Vol.71 (1013), p.369

1979

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Prader-Labhart-Willi syndrome with 47,XXX karyotype. Etio-pathogenetic considerations

Minerva pediatrica, 1986-04, Vol.38 (8), p.271

1986

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Pathology of chromosome 16

Pathologica, 1979-05, Vol.71 (1013), p.362

1979

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Interstitial deletion of 13 (q21 to q31)

Pathologica, 1979-05, Vol.71 (1013), p.359

1979

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Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st report

Minerva pediatrica, 1990-01, Vol.42 (1-2), p.25

1990

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Variability of r(22) Chromosome Phenotypical Expression

Acta geneticae medicae et gemellologiae, 1977-01, Vol.26 (3-4), p.287-290

1977

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P1338: INFUSION OF DIMETHYL SULFOXIDE (DMSO) ‐ DEPLETED AUTOLOGOUS PERIPHERAL BLOOD PROGENITOR CELLS REDUCES POST‐AUTOGRAFTING SEVERE GASTRIC TOXICITIES AND HOSPITALIZATION LENGTH

HemaSphere, 2022-06, Vol.6 (Suppl), p.1223-1224

2022

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A New Carrier for Selective Removal of Heavy Metal Ions from Aqueous Solutions through Bulk Liquid Membranes

European journal of organic chemistry, 2004-09, Vol.2004 (18), p.3865-3871

2004

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Carrier-Mediated Transport of Toxic Heavy Metal Ions in Bulk Liquid Membranes

European journal of organic chemistry, 2004-03, Vol.2004 (6), p.1330-1335

2004

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Antenatal diagnosis of tuberous sclerosis

Increased chromosomal breakage in epileptic children after long-term treatment

Mating between two balanced translocation carriers in two unrelated families

Antenatal diagnosis of tuberous sclerosis

Prenatal diagnosis of deletion 11q23-->qter. Report of two unrelated cases

Identification of the origin of a 22p+ chromosome by triplex dosage effect of LDH B, GAPHD, TPI and ENO2

Infantile Spasms and the CHARGE Association

t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome

Mosaicism 45,X/46,X,r/(Y) associated with mixed gonadal dysgenesis. Description of a case and review of the literature

Fanconi's anemia type Estren-Dameshek. A case report (author's transl)

Ultrastructural and Biological Characterization of Human Choroid Cell Cultures Transformed by Simian Virus 40

Biological and ultrastructural characteristics of a line of human choroid transformed by SV40

Variability of r(22) chromosomes phenotypical expression

2 new cases of chromosome 22 with ring structure

Prader-Labhart-Willi syndrome with 47,XXX karyotype. Etio-pathogenetic considerations

Pathology of chromosome 16

Interstitial deletion of 13 (q21 to q31)

Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st report

Variability of r(22) Chromosome Phenotypical Expression

P1338: INFUSION OF DIMETHYL SULFOXIDE (DMSO) ‐ DEPLETED AUTOLOGOUS PERIPHERAL BLOOD PROGENITOR CELLS REDUCES POST‐AUTOGRAFTING SEVERE GASTRIC TOXICITIES AND HOSPITALIZATION LENGTH

A New Carrier for Selective Removal of Heavy Metal Ions from Aqueous Solutions through Bulk Liquid Membranes

Carrier-Mediated Transport of Toxic Heavy Metal Ions in Bulk Liquid Membranes

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