UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 97

Sortiert nach

Recurrence risk in CHD

Circulation (New York, N.Y.), 1977-03, Vol.55 (3), p.555-556

Zetterqvist, P

1977

Volltextzugriff (PDF)

What is a shunt? Concepts of central shunts and effective flow and a method for graphical presentation of circulatory quantities and their interrelations

Upsala journal of medical sciences. Supplement, 1980, Vol.28, p.1

Zetterqvist, P

1980

Volltextzugriff (PDF)

The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype: Report of 11 patients and delineation of the clinical picture

Human genetics, 1981-04, Vol.57 (2)

1981

Volltextzugriff (PDF)

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

The Journal of thoracic and cardiovascular surgery, 1979-07, Vol.78 (1), p.35-38

1979

Volltextzugriff (PDF)

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

Clinical genetics, 1995-08, Vol.48 (2), p.85-89

1995

Volltextzugriff (PDF)

Congenital Diabetes Mellitus and Neonatal Pseudodiabetes Mellitus

Archives of disease in childhood, 1957-06, Vol.32 (163), p.193-196

1957

Volltextzugriff (PDF)

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

British Heart Journal, 1969-01, Vol.31 (1), p.37-44

1969

Volltextzugriff (PDF)

Aortic Origin of the Right Pulmonary Artery and Wide Patent Ductus Arteriosus

Scandinavian cardiovascular journal : SCJ, 1970, Vol.4 (1), p.87-95

1970

Volltextzugriff (PDF)

Aberrant left pulmonary artery

Acta chirurgica Scandinavica. Supplementum, 1959, Vol.Suppl 245, p.331

1959

Volltextzugriff (PDF)

Total anomalous pulmonary venous connection in siblings. Report on three families

Acta pædiatrica Scandinavica, 1987-01, Vol.76 (1), p.124

1987

Volltextzugriff (PDF)

Clinical and Cytogenetic Investigation in Children of Parents Treated with Radioiodine

Acta oncologica, 1972-01, Vol.11 (3), p.193-208

1972

Volltextzugriff (PDF)

26. THE ETIOLOGY OF PATENT DUCTUS ARTERIOSUS

Acta Paediatrica, 1970-10, Vol.59 (S206), p.42-42

ZETTERQVIST, P.

1970

Volltextzugriff (PDF)

TRISOMY 13-15. REPORT OF A CASE WITH CLINICAL, CYTOGENETIC AND PATHOLOGIC FINDINGS

Acta pathologica et microbiologica Scandinavica, 1964-01, Vol.60 (1), p.36-46

1964

Volltextzugriff (PDF)

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

Acta Paediatrica, 1963-01, Vol.52 (1), p.115-122

ZETTERQVIST, PER

1963

Volltextzugriff (PDF)

The hereditary risks in congenital heart defects

Läkartidningen, 1967-03, Vol.64 (12), p.1207

Zetterqvist, P

1967

Volltextzugriff (PDF)

Is family intermarriage without risks?

Läkartidningen, 1966-10, Vol.63 (43), p.4042

Zetterqvist, P

1966

Volltextzugriff (PDF)

Accumulation of different congenital heart defects in one pedigree

Clinical genetics, 1971-05, Vol.2 (3), p.123-127

Zetterqvist, Per

1971

Volltextzugriff (PDF)

Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings

Annales de génétique, 1971-12, Vol.14 (4), p.275

1971

Volltextzugriff (PDF)

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

Scandinavian cardiovascular journal : SCJ, 1967, Vol.1 (1), p.68-75

Zetterqvist, Per

1967

Volltextzugriff (PDF)

Reflections on the concept "malformation" and its application to pediatric cardiology

Svenska lakartidningen, 1962-11, Vol.59, p.3540

ZETTERQVIST, P

1962

Volltextzugriff (PDF)

Multiple occurrence of atrial septal defect in a family

Acta pædiatrica, 1960-11, Vol.49, p.741

ZETTERQVIST, P

1960

Volltextzugriff (PDF)

Socalled physiological icterus in the premature infant, a hazardous condition

Nordisk medicin, 1957-08, Vol.58 (35), p.1278

ZETTERQVIST, P

1957

Volltextzugriff (PDF)

Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18

Annales de génétique, 1972-06, Vol.15 (2), p.93

1972

Volltextzugriff (PDF)

Medication for Attention Deficit–Hyperactivity Disorder and Criminality

The New England journal of medicine, 2012-11, Vol.367 (21), p.2006-2014

2012

Volltextzugriff (PDF)

Marfan syndrome and dilated aortic root--clinical findings, diagnosis and case reports

Läkartidningen, 1989-06, Vol.86 (23), p.2207

1989

Volltextzugriff (PDF)

1 – 25 von 97

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(73)
Mit Volltextzugriff
(50)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Recurrence risk in CHD

What is a shunt? Concepts of central shunts and effective flow and a method for graphical presentation of circulatory quantities and their interrelations

The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype: Report of 11 patients and delineation of the clinical picture

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

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

Congenital Diabetes Mellitus and Neonatal Pseudodiabetes Mellitus

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

Aortic Origin of the Right Pulmonary Artery and Wide Patent Ductus Arteriosus

Aberrant left pulmonary artery

Total anomalous pulmonary venous connection in siblings. Report on three families

Clinical and Cytogenetic Investigation in Children of Parents Treated with Radioiodine

26. THE ETIOLOGY OF PATENT DUCTUS ARTERIOSUS

TRISOMY 13-15. REPORT OF A CASE WITH CLINICAL, CYTOGENETIC AND PATHOLOGIC FINDINGS

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

The hereditary risks in congenital heart defects

Is family intermarriage without risks?

Accumulation of different congenital heart defects in one pedigree

Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings

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

Reflections on the concept "malformation" and its application to pediatric cardiology

Multiple occurrence of atrial septal defect in a family

Socalled physiological icterus in the premature infant, a hazardous condition

Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18

Medication for Attention Deficit–Hyperactivity Disorder and Criminality

Marfan syndrome and dilated aortic root--clinical findings, diagnosis and case reports

Suchergebnisse filtern