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1
Education in obstetrical ultrasound - an important factor for increasing the prenatal detection of congenital heart disease
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Article
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Education in obstetrical ultrasound - an important factor for increasing the prenatal detection of congenital heart disease

Acta obstetricia et gynecologica Scandinavica, 2013-07, Vol.92 (7), p.804-808 [Peer Reviewed Journal]

2013 Nordic Federation of Societies of Obstetrics and Gynecology ;2013 Nordic Federation of Societies of Obstetrics and Gynecology. ;ISSN: 0001-6349 ;ISSN: 1600-0412 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.12140 ;PMID: 23521227 ;CODEN: AOGSAE

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2
Medical care of adults with congenital heart diseases : Present and future
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Medical care of adults with congenital heart diseases : Present and future

Herz, 2019-09, Vol.44 (6), p.553 [Peer Reviewed Journal]

EISSN: 1615-6692 ;DOI: 10.1007/s00059-019-4820-9 ;PMID: 31263905

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3
The hairless (hr) gene is involved in the congenital hypotrichosis of Valle del Belice sheep
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The hairless (hr) gene is involved in the congenital hypotrichosis of Valle del Belice sheep

Genetics selection evolution (Paris), 2003-06, Vol.35 (Suppl 1), p.S147-S156, Article S147 [Peer Reviewed Journal]

2003 INIST-CNRS ;COPYRIGHT 2003 BioMed Central Ltd. ;INRA, EDP Sciences 2003. ;Copyright ©2003 INRA, EDP Sciences 2003 INRA, EDP Sciences ;ISSN: 0999-193X ;ISSN: 1297-9686 ;EISSN: 1297-9686 ;DOI: 10.1186/1297-9686-35-S1-S147 ;PMID: 12927087

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4
Ankyloglossia in an Anatolian Shepherd dog
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Article
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Ankyloglossia in an Anatolian Shepherd dog

Schweizer Archiv für Tierheilkunde, 2006-08, Vol.148 (8), p.417-420 [Peer Reviewed Journal]

ISSN: 0036-7281 ;DOI: 10.1024/0036-7281.148.8.417 ;PMID: 16933707

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5
Research on Rare Diseases in Germany - The GAIN Registry: a registry for individuals with congenital multi-organ autoimmune diseases
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Article
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Research on Rare Diseases in Germany - The GAIN Registry: a registry for individuals with congenital multi-organ autoimmune diseases

Journal of health monitoring, 2023-12, Vol.8 (4), p.24-30

Robert Koch Institute. All rights reserved unless explicitly granted. ;Robert Koch Institute. All rights reserved unless explicitly granted. 2023 ;EISSN: 2511-2708 ;DOI: 10.25646/11732 ;PMID: 38235015

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6
Adults with congenital heart disease: treatment and medical problems
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Article
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Adults with congenital heart disease: treatment and medical problems

Herz, 2013-09, Vol.38 (6), p.639-654 [Peer Reviewed Journal]

ISSN: 0340-9937 ;EISSN: 1615-6692 ;DOI: 10.1007/s00059-013-3927-7 ;PMID: 23942735

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7
Congenital fibrosis of extraocular muscles (CFEOM) and other phenotypes of congenital cranial dysinnervation syndromes (CCDD)
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Article
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Congenital fibrosis of extraocular muscles (CFEOM) and other phenotypes of congenital cranial dysinnervation syndromes (CCDD)

Nervenarzt, 2005-04, Vol.76 (4), p.395-402 [Peer Reviewed Journal]

EISSN: 1433-0407 ;DOI: 10.1007/s00115-004-1742-3 ;PMID: 15221064

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8
A new approach to the interpretation of B-type natriuretic peptide concentration in children with congenital heart disease
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Article
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A new approach to the interpretation of B-type natriuretic peptide concentration in children with congenital heart disease

Journal of laboratory medicine, 2023-10, Vol.47 (5), p.225-232 [Peer Reviewed Journal]

ISSN: 2567-9430 ;EISSN: 2567-9449 ;DOI: 10.1515/labmed-2022-0150

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9
Prenatal diagnosis of congenital heart diseases by fetal echocardiography in second trimester: a Chinese multicenter study
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Prenatal diagnosis of congenital heart diseases by fetal echocardiography in second trimester: a Chinese multicenter study

Acta obstetricia et gynecologica Scandinavica, 2017-04, Vol.96 (4), p.454-463 [Peer Reviewed Journal]

2016 Nordic Federation of Societies of Obstetrics and Gynecology ;2016 Nordic Federation of Societies of Obstetrics and Gynecology. ;Copyright © 2017 Acta Obstetricia et Gynecologica Scandinavica ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.13085 ;PMID: 28029179 ;CODEN: AOGSAE

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10
Catheter Interventions in Congenital Heart Disease – Hot Topics 2013
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Conference Proceeding
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Catheter Interventions in Congenital Heart Disease – Hot Topics 2013

The Thoracic and Cardiovascular Surgeon, 2013 [Peer Reviewed Journal]

ISSN: 0171-6425 ;EISSN: 1439-1902 ;DOI: 10.1055/s-0033-1354491

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11
Characterization of the porcine CDKN3 gene as a potential candidate for congenital splay leg in piglets
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Article
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Characterization of the porcine CDKN3 gene as a potential candidate for congenital splay leg in piglets

Genetics selection evolution (Paris), 2003-06, Vol.35 (Suppl 1), p.S157-S165, Article S157 [Peer Reviewed Journal]

2003 INIST-CNRS ;COPYRIGHT 2003 BioMed Central Ltd. ;INRA, EDP Sciences 2003. ;Copyright ©2003 INRA, EDP Sciences 2003 INRA, EDP Sciences ;ISSN: 0999-193X ;ISSN: 1297-9686 ;EISSN: 1297-9686 ;DOI: 10.1186/1297-9686-35-S1-S157 ;PMID: 12927088

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12
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
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Article
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X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle

Genetics selection evolution (Paris), 2003-06, Vol.35 (Suppl 1), p.S137-S145, Article S137 [Peer Reviewed Journal]

2003 INIST-CNRS ;COPYRIGHT 2003 BioMed Central Ltd. ;INRA, EDP Sciences 2003. ;Copyright ©2003 INRA, EDP Sciences 2003 INRA, EDP Sciences ;ISSN: 0999-193X ;ISSN: 1297-9686 ;EISSN: 1297-9686 ;DOI: 10.1186/1297-9686-35-S1-S137 ;PMID: 12927086

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13
2020 ESC guidelines on treatment of adult congenital heart disease (ACHD)
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Article
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2020 ESC guidelines on treatment of adult congenital heart disease (ACHD)

Herz, 2021-02, Vol.46 (1), p.14 [Peer Reviewed Journal]

EISSN: 1615-6692 ;DOI: 10.1007/s00059-020-05003-0 ;PMID: 33258988

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14
Congenital bone marrow failure syndromes. The last 20 years by the example of congenital neutropenia
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Article
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Congenital bone marrow failure syndromes. The last 20 years by the example of congenital neutropenia

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2007-12, Vol.50 (12), p.1564-1568 [Peer Reviewed Journal]

ISSN: 1436-9990 ;EISSN: 1437-1588 ;DOI: 10.1007/s00103-007-0392-6 ;PMID: 18026880

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15
AHA level of care classification in congenital heart disease in a German Heart Center – a single center retrospective observational study
Material Type:
Conference Proceeding
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AHA level of care classification in congenital heart disease in a German Heart Center – a single center retrospective observational study

Geburtshilfe und Frauenheilkunde, 2022, Vol.82 (10) [Peer Reviewed Journal]

Thieme. All rights reserved. ;ISSN: 0016-5751 ;EISSN: 1438-8804 ;DOI: 10.1055/s-0042-1756848

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16
Added value of prenatal array Comparative Genomic Hybridization (aCGH) in fetuses with congenital heart disease: a single-center experience
Material Type:
Conference Proceeding
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Added value of prenatal array Comparative Genomic Hybridization (aCGH) in fetuses with congenital heart disease: a single-center experience

Geburtshilfe und Frauenheilkunde, 2022, Vol.82 (10) [Peer Reviewed Journal]

Thieme. All rights reserved. ;ISSN: 0016-5751 ;EISSN: 1438-8804 ;DOI: 10.1055/s-0042-1757112

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17
Neues und Bewährtes zur Arbeit, Diagnostik und Therapie der Anämien im Kindesund Jugendalter
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Article
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Neues und Bewährtes zur Arbeit, Diagnostik und Therapie der Anämien im Kindesund Jugendalter

Nieren- und Hockdruckkrankheiten, 2023-07, Vol.52 (7), p.283 [Peer Reviewed Journal]

Copyright Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG 2023 ;ISSN: 0300-5224 ;DOI: 10.5414/NHX02309

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18
Outcome in newborns with intervention < 48 hours postpartum in prenatally versus postnatally diagnosed congenital heart disease
Material Type:
Conference Proceeding
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Outcome in newborns with intervention < 48 hours postpartum in prenatally versus postnatally diagnosed congenital heart disease

Ultraschall in der Medizin - European Journal of Ultrasound, 2016 [Peer Reviewed Journal]

ISSN: 0172-4614 ;EISSN: 1438-8782 ;DOI: 10.1055/s-0036-1587795

Digital Resources/Online E-Resources

19
Point shear wave elastography in congenital metabolic liver diseases
Material Type:
Conference Proceeding
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Point shear wave elastography in congenital metabolic liver diseases

Ultraschall in der Medizin - European Journal of Ultrasound, 2016 [Peer Reviewed Journal]

ISSN: 0172-4614 ;EISSN: 1438-8782 ;DOI: 10.1055/s-0036-1587849

Digital Resources/Online E-Resources

20
Mutation of the MYH3 gene causes recessive cleft palate in Limousine cattle
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Article
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Mutation of the MYH3 gene causes recessive cleft palate in Limousine cattle

Genetics selection evolution (Paris), 2022-10, Vol.54 (1), p.71-71, Article 71 [Peer Reviewed Journal]

COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Attribution ;The Author(s) 2022 ;ISSN: 1297-9686 ;ISSN: 0999-193X ;EISSN: 1297-9686 ;DOI: 10.1186/s12711-022-00762-2 ;PMID: 36309651

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