Cytogenetic investigations in families with ataxia-telangiectasia.

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.

Clinical, cytogenetic and molecular investigations in three patients with Wolf-Hirschhorn syndrome.

Investigations of Ramachandran disallowed conformations in protein domain families.

Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family.

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families.

Cytogenetic investigations on a cell line derived from a carcinoma arising in a salivary gland pleomorphic adenoma.

Cytogenetic studies in gonadal dysgenesis with dysgerminoma.

Drug interference with laboratory investigations.

Catamnestic investigations in children with congenital hydrocephalus.

Cytogenetic abnormalities associated with renal cell carcinoma.

Cytogenetic studies in myelomatosis.

Triadic Interactions in Families of Adolescents with Anorexia Nervosa and Families of Adolescents with Internalizing Disorders.

Cytogenetic characterization of three Balistoidea fish species from the Atlantic with inferences on chromosomal evolution in the families Monacanthidae and Balistidae.

Echinocytes in families with Duchenne muscular dystrophy.

Alexithymia and depression in families with alcoholics.

Biological liability in families with autism.

Childhood psychopathology in families with multigenerational alcoholism.

HLA--determination in families with hereditary ataxia.

Actinobacillus actinomycetemcomitans in families afflicted with periodontitis.

Cancers in 44 families with ataxia-telangiectasia.

Cytogenetic biomonitoring in oral leukoplakia patients with mild dysplasia.

Cytogenetic investigation in 413 couples with spontaneous abortions.

Cytogenetic analysis in ataxia telangiectasia with malignant lymphoma.

Cytogenetic studies in seven individuals with an i(Xq) karyotype.

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Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.

Clinical, cytogenetic and molecular investigations in three patients with Wolf-Hirschhorn syndrome.

Investigations of Ramachandran disallowed conformations in protein domain families.

Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family.

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families.

Cytogenetic investigations on a cell line derived from a carcinoma arising in a salivary gland pleomorphic adenoma.

Cytogenetic studies in gonadal dysgenesis with dysgerminoma.

Drug interference with laboratory investigations.

Catamnestic investigations in children with congenital hydrocephalus.

Cytogenetic abnormalities associated with renal cell carcinoma.

Cytogenetic studies in myelomatosis.

Triadic Interactions in Families of Adolescents with Anorexia Nervosa and Families of Adolescents with Internalizing Disorders.

Cytogenetic characterization of three Balistoidea fish species from the Atlantic with inferences on chromosomal evolution in the families Monacanthidae and Balistidae.

Echinocytes in families with Duchenne muscular dystrophy.

Alexithymia and depression in families with alcoholics.

Biological liability in families with autism.

Childhood psychopathology in families with multigenerational alcoholism.

HLA--determination in families with hereditary ataxia.

Actinobacillus actinomycetemcomitans in families afflicted with periodontitis.

Cancers in 44 families with ataxia-telangiectasia.

Cytogenetic biomonitoring in oral leukoplakia patients with mild dysplasia.

Cytogenetic investigation in 413 couples with spontaneous abortions.

Cytogenetic analysis in ataxia telangiectasia with malignant lymphoma.

Cytogenetic studies in seven individuals with an i(Xq) karyotype.

Cytogenetic investigations in families with ataxia-telangiectasia.

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