المؤلفون: Fraser FC; Department of Human Genetics, McGill University, Montreal, Quebec, Canada., Teebi AS, Walsh S, Pinsky L

المصدر: American journal of medical genetics [Am J Med Genet] 1997 Dec 12; Vol. 73 (2), pp. 194-6.

نوع المنشور: Case Reports; Journal Article; Review

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia* , Poland Syndrome*, Female ; Humans ; Infant, Newborn ; Male

المؤلفون: Nachlieli T; Department of Pediatrics A, Rambam Medical Center, Haifa, Israel., Gershoni-Baruch R

المصدر: American journal of medical genetics [Am J Med Genet] 1992 Feb 15; Vol. 42 (4), pp. 458-60.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia* , Microphthalmos*, Abnormalities, Multiple/*pathology, Athetosis ; Cleft Palate ; Consanguinity ; Genes, Recessive ; Humans ; Infant, Newborn ; Intellectual Disability ; Male ; Syndrome

المؤلفون: Murphy EA; Center for Medical Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland., Rhee S, Pyeritz RE, Berger KR

المصدر: American journal of medical genetics [Am J Med Genet] 1991 Dec 01; Vol. 41 (3), pp. 362-70.

نوع المنشور: Journal Article; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Linear Models* , Models, Biological*, Dextrocardia/*embryology , Homeostasis/*physiology , Morphogenesis/*physiology, Dextrocardia/genetics ; Humans

المؤلفون: Agirbasli M; Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA., Hamid R, Jennings HS 3rd, Tiller GE

المصدر: American journal of medical genetics [Am J Med Genet] 2000 Apr 24; Vol. 91 (5), pp. 327-30.

نوع المنشور: Journal Article; Twin Study

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Cardiomyopathy, Hypertrophic*/etiology , Cardiomyopathy, Hypertrophic*/physiopathology , Diseases in Twins* , Situs Inversus*/complications , Situs Inversus*/physiopathology, Adult ; Age of Onset ; Dextrocardia/etiology ; Female ; Humans ; Twins, Monozygotic

المؤلفون: Aughton DJ; Department of Pediatrics, William Beaumont Hospital, Royal Oak, Michigan, MI 48072.

المصدر: American journal of medical genetics [Am J Med Genet] 1990 Oct; Vol. 37 (2), pp. 178-81.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Abnormalities, Multiple/*genetics , Anophthalmos/*genetics , Bone and Bones/*abnormalities , Dextrocardia/*genetics, Consanguinity ; Face/abnormalities ; Humans ; Infant, Newborn ; Male ; Ribs/abnormalities ; Spine/abnormalities ; Syndrome

المؤلفون: Distefano G; Department of Pediatrics, University of Catania, Italy., Romeo MG, Grasso S, Mazzone D, Sciacca P, Mollica F

المصدر: American journal of medical genetics [Am J Med Genet] 1987 Aug; Vol. 27 (4), pp. 929-34.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Abnormalities, Multiple/*diagnostic imaging , Dextrocardia/*diagnostic imaging , Heart Defects, Congenital/*diagnostic imaging , Lung/*abnormalities , Spleen/*abnormalities , Transposition of Great Vessels/*diagnostic imaging , Viscera/*abnormalities, Consanguinity ; Female ; Genes, Recessive ; Humans ; Infant, Newborn ; Lung/diagnostic imaging ; Male ; Radiography ; Spleen/diagnostic imaging ; Syndrome ; Viscera/diagnostic imaging

المؤلفون: Stratton RF; Department of Pediatrics, Wilford Hall United States Air Force Medical Center, Lackland Air Force Base, Texas 78236-5300., Parker MW

المصدر: American journal of medical genetics [Am J Med Genet] 1989 Feb; Vol. 32 (2), pp. 169-73.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print) Linking ISSN: 01487299 NLM ISO Abbreviation: Am J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Bone Diseases, Developmental/*genetics , Dextrocardia/*genetics , Fingers/*abnormalities , Growth Hormone/*deficiency , Heart Defects, Congenital/*genetics, Abnormalities, Multiple/genetics ; Anus, Imperforate/genetics ; Child Development ; Contracture/genetics ; Cryptorchidism/genetics ; Ductus Arteriosus, Patent/genetics ; Humans ; Hypospadias/genetics ; Infant ; Male

المؤلفون: Volkan Baltaci, Kürşat Tokel, Arda Saygili, Zerrin Yilmaz, Murat Derbent, Birgül Varan

المصدر: American Journal of Medical Genetics. :129-135

مصطلحات موضوعية: Heart Defects, Congenital, Male, congenital, hereditary, and neonatal diseases and abnormalities, Turkey, Chromosomes, Human, Pair 22, Heart Ventricles, Aorta, Thoracic, Double outlet right ventricle, Ductus arteriosus, Humans, Medicine, Child, Genetics (clinical), Tetralogy of Fallot, Dextrocardia, business.industry, Infant, Arteries, Anatomy, Transposition of the great vessels, medicine.disease, Situs inversus, Phenotype, medicine.anatomical_structure, Great arteries, Child, Preschool, Female, Sacral dimple, Chromosome Deletion, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c135fd3a8028dbc4b1f1c4962b9d7013
https://doi.org/10.1002/ajmg.a.10832

المؤلفون: Mehmet Agirbasli, George E. Tiller, Henry S. Jennings Iii, Rizwan Hamid

المصدر: American Journal of Medical Genetics. 91:327-330

مصطلحات موضوعية: Dextrocardia, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Heart disease, business.industry, Situs viscerum inversus, fungi, Hypertrophic cardiomyopathy, Monozygotic twin, medicine.disease, Situs inversus, Endocrinology, Internal medicine, otorhinolaryngologic diseases, medicine, Cardiology, Congenital disease, Identical twins, business, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::214c92466eb134683cefbcefa67056db
https://doi.org/10.1002/(sici)1096-8628(20000424)91:5<327::aid-ajmg1>3.0.co;2-s

المؤلفون: K.S. Reddy, David B. Flannery, R. James Farrer

المصدر: American Journal of Medical Genetics. 84:460-468

مصطلحات موضوعية: Dextrocardia, congenital, hereditary, and neonatal diseases and abnormalities, business.industry, Abdominal Hernia, Anatomy, medicine.disease, Descending colon, medicine.anatomical_structure, Situs, Atresia, otorhinolaryngologic diseases, medicine, Ascending colon, Abdomen, Hernia, business, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::71346754904b80f13e9ec6d01d12c99d
https://doi.org/10.1002/(sici)1096-8628(19990611)84:5<460::aid-ajmg10>3.0.co;2-l