Related Experiment Videos
Prune belly syndrome in two siblings and a first cousin. Possible genetic implications
American Journal of Diseases of Children (1960)
|January 1, 1982
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Stroke in Nigerian children with sickle cell disease.
African journal of medicine and medical sciences·2006
HIV-assocated lymphoma: a case report.
African journal of medicine and medical sciences·2003
Deficiencies in tetanus prophylaxis in wound management in Ibadan, Nigeria.
West African journal of medicine·2002
Injection-induced sciatic nerve injury in Nigerian children.
The Central African journal of medicine·2002
Hyperventilation-precipitated cerebrovascular accident in a patient with sickle cell anaemia.
African journal of medicine and medical sciences·2001
Applicability of the Greulich and Pyle skeletal age standards to black and white children of today.
American journal of diseases of children (1960)·1993
Maltreatment of children born to cocaine-dependent mothers.
American journal of diseases of children (1960)·1993
Adrenal tumor complicating untreated 21-hydroxylase deficiency in a 5 1/2-year-old boy.
American journal of diseases of children (1960)·1993
Passive-active immunization in infants of hepatitis Be antigen-positive mothers. Comparison of the efficacy of early and delayed active immunization.
American journal of diseases of children (1960)·1993
Effects of methylphenidate on sleep in children with attention-deficient hyperactivity disorder. An activity monitor study.
American journal of diseases of children (1960)·1993
Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism. Micro syndrome.
American journal of diseases of children (1960)·1993
Integrative Principal Component-QTL Mapping Identifies Genetic Modifiers of Tumor and Metabolic Traits in Smad4-Deficient Collaborative Cross Mice.
International journal of molecular sciences·2026
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.
American journal of medical genetics. Part A·2026
Wilson disease associated with a novel variant in the ATP7B gene.
Frontiers in neurology·2026