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Volume 16 Number
Familial t413 With Abnormal Offspring in Three Generations
A Syndrome Combining an Acrorenal Field Defect Ectodermal
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3-galactosidase abnormalities abortions achondroplasia acid Address reprint requests Alan allele amniocentesis analysis anomalies ascertainment asplenia autosomal Birth Defects blood carriers cells centile child CHRS Clin Genet clinical congenital consanguineous cytogenetic deficiency disease disorder dominant Duchenne muscular dystrophy dysplasia enzyme female fetal fibroblasts fragile fragile site Freire-Maia gene frequency genotype Hospital Hum Genet hypertelorism hypoplasia hypoplastic inbred inbreeding increased individuals infants inheritance levels Liss liveborn locus Lp(a male malformations marker maternal Medical Genetics metabolic Morquio multiple mutation neonatal nondisjunction normal Opitz P(Aa:Aa parents patients Pediatrics pedigree phenotype pipecolic acid Plecker polysplenia population pregnancy prenatal diagnosis probability radiographic Received for publication recessive reciprocal translocation relatives reported requests to Dr retardation revision received ring chromosome Robertsonian translocation sample score segregation serum showed sibships significant Sikh situs inversus syndrome Table trait trisomy University variables