P. Zetterqvist

发表

The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

J. Opitz, R. Tenconi, J. Lindsten, 1981, Human genetics.

Late results after surgical closure of ventricular septal defect in children.

V. Björk, A. Boccanelli, P. Zetterqvist, 1980, Scandinavian journal of thoracic and cardiovascular surgery.

Ventricular dynamics after surgical closure of VSD.

A. Boccanelli, P. Zetterqvist, C. G. Wallgren, 1980, Scandinavian journal of thoracic and cardiovascular surgery.

II. CARDIAC OUTPUT STUDIES IN INFANTS AND CHILDREN UNDERGOING RIGHT HEART CATHETERIZATION

P. Zetterqvist, C. G. Wallgren, G. Kretzschmar, 1975, Acta paediatrica Scandinavica. Supplement.

Hemodynamic features of extrasystoles in newborn and older infants.

I. Gessner, W. Oh, R. Arcilla, 1966, The American journal of cardiology.

Noonan syndrome with café‐au‐lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus

G. Annéren, N. Dahl, P. Zetterqvist, 1995, Clinical genetics.

Atypical coarctation of the aorta with bilateral vertebral-subclavian pathway. A report of the first known case of preligamental aortic arch interruption and its surgical correction.

P. Zetterqvist, 1967, Scandinavian journal of thoracic and cardiovascular surgery.

Recurrence risk in CHD.

P. Zetterqvist, 1977, Circulation.

Clinical and cytogenetic investigation in children of parents treated with radioiodine.

J. Lindsten, M. Hultén, P. Zetterqvist, 1972, Acta radiologica: therapy, physics, biology.

The “Cat Eye syndrome”: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter→q11) associated with a characteristic phenotype

J. Opitz, R. Tenconi, J. Lindsten, 1981, Human Genetics.

Post‐Mortein Diagnosis of a New Double‐Trisomy Associated With Cardiovascular and Other Anomalies 1

B. Ivemark, K. Gustavson, P. Zetterqvist, 1962 .

TRANSLOCATION HETEROZYGOSITY IN MAN

P. Zetterqvist, J. Böök, B. Santesson, 1961 .

Association Between Congenital Heart Malformation and Chromosomal Variations 1

P. Zetterqvist, J. Böök, B. Santesson, 1959 .

Association Between Congenital Heart Malformation and Chromosomal Variations 1

P. Zetterqvist, J. Böök, B. Santesson, 1961 .

Aortic origin of the right pulmonary artery and wide patent ductus arteriosus.

U. Rudhe, V. Björk, P. Zetterqvist, 1970, Scandinavian journal of thoracic and cardiovascular surgery.

Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms

N. Tommerup, K. Brøndum‐Nielsen, M. Petersen, 1996, Human Genetics.

MALIGNANT PHEOCHROMOCYTOMA IN A CHILD: TREATMENT WITH A COMBINATION OF ALPHA‐ AND BETA‐ADRENERGIC BLOCKADE

U. Broberger, P. Zetterqvist, L. Boréus, 1968, Acta paediatrica Scandinavica.

Dominant mode of inheritance in atrial septal defect

N. Ohlsson, I. Turesson, B. Johansson, 1971, Clinical genetics.

Multiple Occurrence of Atrial Septal Defect in a Family

P. Zetterqvist, 1960, Acta paediatrica.

Long-term treatment with propranolol in selected cases of Fallot's tetralogy.

B. Eriksson, P. Zetterqvist, C. Thorén, 1969, British heart journal.

The Syndrome of Familial Atrial Septal Defect, Heart Arrhythmia and Hand Malformation (Holt‐Oram) in Mother and Son

P. Zetterqvist, 1963 .

Aberrant left pulmonary artery.

U. Rudhe, P. Zetterqvist, 1959, Acta chirurgica Scandinavica. Supplementum.

Successful surgical treatment of an aortico--left ventricular tunnel in a four-month-old infant.

V. Björk, P. Zetterqvist, O. Eklöf, 1979, The Journal of thoracic and cardiovascular surgery.

Aortic Hypoplasia

P. Zetterqvist, O. Eklöf, D. O. Ilha, 1964, Acta paediatrica.

Congenital Diabetes Mellitus and Neonatal Pseudodiabetes Mellitus

P. Zetterqvist, G. Engleson, 1957, Archives of disease in childhood.

Accumulation of different congenital heart defects in one pedigree

P. Zetterqvist, 1971, Clinical genetics.

MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.

H. Klinger, J. Lindsten, M. Fraccaro, 1965, Cytogenetics.

Clinical experience of pacemaker treatment in children.

S. Pehrsson, R. Nordlander, P. Zetterqvist, 1992, Scandinavian journal of thoracic and cardiovascular surgery.

V. EXERCISE STUDIES IN CHILDREN WITH CONGENITAL HEART DISEASE. AN EARPIECE DENSITOMETRIC INVESTIGATION

P. Zetterqvist, C. G. Wallgren, G. Kretzschmar, 1975, Acta paediatrica Scandinavica. Supplement.

Complete Atrioventricular Canal. Long Term Results With Special Reference to Block and Mitral Valve Function

V. Björk, C. Thorén, P. Zetterqvist, 1981 .

Chronic Supraventricular Tachycardia of Continuous or Repetitive Type in Children A Note on Circulatory Function and Long‐Term Prognosis

G. Ström, P. Zetterqvist, E. Zetterqvist, 1960 .

I. VALIDITY OF DICHROMATIC EARPIECE DENSITOMETRY FOR QUANTITATIVE STUDIES IN CHILDREN WITH SHUNT‐FREE CARDIOVASCULAR MALFORMATIONS

J. Hanson, P. Zetterqvist, G. Kretzschmar, 1975, Acta paediatrica Scandinavica. Supplement.

Post-mortem diagnosis of a new double-trisomy associated with cardiovascular and other anomalies.

B. Ivemark, K. Gustavson, P. Zetterqvist, 1962, Acta paediatrica.

Total Anomalous Pulmonary Venous Connection in Siblings

P. Zetterqvist, K. Sabel, PER ZETTERQVIST, 1987, Acta paediatrica Scandinavica.

Congenital Diabetes Mellitus and Neonatal Pseudodiabetes Mellitus

P. Zetterqvist, G. Engleson, 1957, Archives of disease in childhood.

Fibroma in the interventricular septum of the heart. Successful removal in a 13-month-old infant.

U. Rudhe, V. Björk, P. Zetterqvist, 1967, Scandinavian journal of thoracic and cardiovascular surgery.