Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis

A. Bou�, Fran�oise Muller, C Nézelof, +5

Human Genetics

PediatricsDiagnosisMaternal HealthGynecologyPrenatal Diagnosis +5

Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families

Joan Enric Torra‐Bou, Jean‐Louis Taillemite, P. Hazael-Massieux, +2

Human Genetics

InfertilityPericentric InversionFertilityCytogeneticsGenetic Disorder +12

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics

J.L. Serre, Brigitte Simon‐Bouy, Étienne Mornet, +6

Human Genetics

Genetic TestingMendelian DisorderGenetic DisorderMedicineGenetics +9

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination

Étienne Mornet, Joan Enric Torra‐Bou, Marie Charles Raux-Demay, +6

Human Genetics

MedicineGeneticsLinkage AnalysisGynecologyMaternal Health +8

Identification of the origin of triploidy by HLA markers

P Couillin, J Hors, Joan Enric Torra‐Bou, +1

Human Genetics

HistocompatibilityBiologyHuman Leukocyte AntigenCytogeneticsGenetics +6

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

Étienne Mornet, P. Couillin, F. Kutten, +5

Human Genetics

21-Oh DeficiencyMendelian DisorderClinical FormsGenetic DisorderGenetics +7

Gene dosage effect in human triploid fibroblasts

Claudine Junien, Henriette Rubinson, J C Dreyfus, +4

Human Genetics

Gene TherapiesFibrosisGenetic DisorderGene Dosage EffectHematology +2

Androgenetic origin of African complete hydatidiform moles demonstrated by HLA markers

P Couillin, J M Afoutou, Oumar Faye, +3

Human Genetics

BiologyGeneticsAndrogenetic OriginPathologyMolecular Genetics +4

Prenatal diagnosis of Krabbe disease

Marie T. Vanier, Lars Svennerholm, Jan‐Eric Månsson, +3

Clinical Genetics