J. Winberg

发表

AN EPIDEMIOLOGICAL STUDY OF HYPOSPADIAS IN SWEDEN

B. Källén, J. Winberg, J. Winberg, 1982, Acta paediatrica Scandinavica. Supplement.

DEALING WITH SUSPICIONS OF MALFORMATION FREQUENCY INCREASE: Experience with the Swedish Register of Congenital Malformations

B. Källén, J. Winberg, 1979, Acta paediatrica Scandinavica. Supplement.

Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability.

L. Levin, H. Helgadottir, A. Nordgren, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Multiple malformations studied with a national register of malformations.

B. Källén, J. Winberg, 1969, Pediatrics.

Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome.

J. Winberg, A. Nordenskjöld, F. Arnberg, 2011, Journal of pediatric surgery.

Chimerism resulting from parthenogenetic activation and dispermic fertilization

A. Nordgren, E. Blennow, M. Bondeson, 2010, American journal of medical genetics. Part A.

A Swedish register of congenital malformations. Experience with continuous registration during 2 years with special reference to multiple malformations.

B. Källén, J. Winberg, 1968, Pediatrics.

Caudal mesoderm pattern of anomalies: from renal agenesis to sirenomelia.

B. Källén, J. Winberg, J. Winberg, 1974, Teratology.

Infants with congenital limb reduction registered in the Swedish Register of Congenital Malformations.

B. Källén, J. Winberg, T. Rahmani, 1984, Teratology.

Surveillance of malformations at birth: a comparison of two record systems run in parallel.

B. Källén, A. Ericson, J. Winberg, 1977, International journal of epidemiology.

Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association

A. Nordgren, G. Annéren, E. Sahlin, 2014, PloS one.

Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy

M. Anderberg, J. Winberg, A. Nordenskjöld, 2022, American journal of medical genetics. Part A.

No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations.

A. Nordgren, H. Berggren, J. Winberg, 2015, European journal of medical genetics.

Partial tetrasomy 14 associated with multiple malformations

A. Nordgren, C. Graff, B. Anderlid, 2013, American journal of medical genetics. Part A.

Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformations

A. Nordgren, E. Sahlin, J. Winberg, 2019, Molecular genetics & genomic medicine.

Potassium-, Uranium- and Thorium-concentrations in bedrock. A study of the Sahlgrenska Anomaly and Änggårdsbergen, Gothenburg

J. Winberg, F. Elf, 2019 .