UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 87

Sortiert nach

Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-10, Vol.23 (10), p.1793-1806

2021

Link zum Volltext

Verfügbarkeit prüfen

Response to Prensky and Persson

Genetics in medicine, 2023-09, Vol.25 (9), p.100873-100873, Article 100873

2023

Link zum Volltext

Verfügbarkeit prüfen

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2023-02, Vol.25 (2), p.100336-100336, Article 100336

2023

Link zum Volltext

Verfügbarkeit prüfen

Response to Righetti et al

Genetics in medicine, 2022-05, Vol.24 (5), p.1162-1163

2022

Link zum Volltext

Verfügbarkeit prüfen

Laboratory testing for preconception/prenatal carrier screening: A technical standard of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2024-05, p.101137-101137, Article 101137

2024

Link zum Volltext

Verfügbarkeit prüfen

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2023-08, Vol.25 (8), p.100874-100874, Article 100874

2023

Link zum Volltext

Verfügbarkeit prüfen

Expanded carrier screening: what the reproductive endocrinologist needs to know

Fertility and sterility, 2018-02, Vol.109 (2), p.183-189

Dungan, Jeffrey

2018

Link zum Volltext

Verfügbarkeit prüfen

Correction to: Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-10, Vol.23 (10), p.2015-2015

2021

Link zum Volltext

Verfügbarkeit prüfen

Addendum: Statement on informed consent for medical photographs

Genetics in medicine, 2022-11, Vol.24 (11), p.2413

Dungan, Jeffrey S.

2022

Link zum Volltext

Verfügbarkeit prüfen

Addendum: Preconception and prenatal testing of biologic fathers for carrier status; Carrier screening in individuals of Ashkenazi Jewish descent; Carrier screening for spinal muscular atrophy

Genetics in medicine, 2022-11, Vol.24 (11), p.2414

Dungan, Jeffrey S.

2022

Link zum Volltext

Verfügbarkeit prüfen

Role of the 3‐Vessel and Trachea View in Antenatal Detection of Tetralogy of Fallot

Journal of ultrasound in medicine, 2016-08, Vol.35 (8), p.1799-1809

2016

Link zum Volltext

Verfügbarkeit prüfen

Invasive Prenatal Diagnosis After Positive Cell-Free Fetal DNA Compared With Sequential Prenatal Screening

Obstetrics and gynecology (New York. 1953), 2014-05, Vol.123 Suppl 1 (Supplement 1), p.41S-41S

2014

Link zum Volltext

Verfügbarkeit prüfen

CEVL interactive – “1-Voice”: Shared checklist for prenatal urological consultation

Journal of pediatric urology, 2018-04, Vol.14 (2), p.92-96

2018

Link zum Volltext

Verfügbarkeit prüfen

Testing for Familial BRCA1–2 Mutations: Implications for Genetic Counseling and Risk Assessment

Obstetrics and gynecology (New York. 1953), 2014-05, Vol.123 Suppl 1 (Supplement 1), p.185S-186S

2014

Link zum Volltext

Verfügbarkeit prüfen

“1 Voice” triages care by algorithm for newborn urological ultrasound findings

Journal of pediatric urology, 2018-02, Vol.14 (1), p.6-8

2018

Link zum Volltext

Verfügbarkeit prüfen

“1 Voice”: Learn urinary tract dilation (UTD) classification to assess fetal & newborn urological ultrasound findings

Journal of pediatric urology, 2017-12, Vol.13 (6), p.559-562

2017

Link zum Volltext

Verfügbarkeit prüfen

Carrier screening for cystic fibrosis

Obstetrics and gynecology clinics of North America, 2010-03, Vol.37 (1), p.47

Dungan, Jeffrey S

2010

Link zum Volltext

Verfügbarkeit prüfen

In the nick of time: Despite 2 treatments a cervical ectopic pregnancy continued to advance

American journal of obstetrics and gynecology, 2012-05, Vol.206 (5), p.450.e1-450.e2

2012

Link zum Volltext

Verfügbarkeit prüfen

Characterizing expanded carrier screen results of females whose male partners did not follow through

Molecular genetics and metabolism, 2021-04, Vol.132, p.S308

2021

Link zum Volltext

Verfügbarkeit prüfen

Creating a rational list of X-linked disorders for inclusion on reproductive carrier screening panels

Molecular genetics and metabolism, 2021-04, Vol.132, p.S321

2021

Link zum Volltext

Verfügbarkeit prüfen

eP500 - Creating a rational list of X-linked disorders for inclusion on reproductive carrier screening panels

Molecular genetics and metabolism, 2021-04, Vol.132, p.S321-S321

2021

Link zum Volltext

Verfügbarkeit prüfen

OP478 - Characterizing expanded carrier screen results of females whose male partners did not follow through

Molecular genetics and metabolism, 2021-04, Vol.132, p.S308-S308

2021

Link zum Volltext

Verfügbarkeit prüfen

3-D ultrasound of the fetal ear and fetal autosomal trisomies: a pilot study of a new screening protocol

Prenatal diagnosis, 2011-03, Vol.31 (3), p.311-314

2011

Link zum Volltext

Verfügbarkeit prüfen

In the nick of time

American journal of obstetrics and gynecology, 2012-05, Vol.206 (5), p.450.e1-450.e2

2012

Link zum Volltext

Verfügbarkeit prüfen

Provision of reproductive and cancer genetics services during COVID-19 pandemic

Molecular genetics and metabolism, 2021-04, Vol.132, p.S358-S358

2021

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 87

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(80)
Mit Volltextzugriff
(74)

Publikationsform

Sprache

Englisch
(87)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

Response to Prensky and Persson

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

Response to Righetti et al

Laboratory testing for preconception/prenatal carrier screening: A technical standard of the American College of Medical Genetics and Genomics (ACMG)

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

Expanded carrier screening: what the reproductive endocrinologist needs to know

Correction to: Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

Addendum: Statement on informed consent for medical photographs

Addendum: Preconception and prenatal testing of biologic fathers for carrier status; Carrier screening in individuals of Ashkenazi Jewish descent; Carrier screening for spinal muscular atrophy

Role of the 3‐Vessel and Trachea View in Antenatal Detection of Tetralogy of Fallot

Invasive Prenatal Diagnosis After Positive Cell-Free Fetal DNA Compared With Sequential Prenatal Screening

CEVL interactive – “1-Voice”: Shared checklist for prenatal urological consultation

Testing for Familial BRCA1–2 Mutations: Implications for Genetic Counseling and Risk Assessment

“1 Voice” triages care by algorithm for newborn urological ultrasound findings

“1 Voice”: Learn urinary tract dilation (UTD) classification to assess fetal & newborn urological ultrasound findings

Carrier screening for cystic fibrosis

In the nick of time: Despite 2 treatments a cervical ectopic pregnancy continued to advance

Characterizing expanded carrier screen results of females whose male partners did not follow through

Creating a rational list of X-linked disorders for inclusion on reproductive carrier screening panels

eP500 - Creating a rational list of X-linked disorders for inclusion on reproductive carrier screening panels

OP478 - Characterizing expanded carrier screen results of females whose male partners did not follow through

3-D ultrasound of the fetal ear and fetal autosomal trisomies: a pilot study of a new screening protocol

In the nick of time

Provision of reproductive and cancer genetics services during COVID-19 pandemic

Suchergebnisse filtern