Suchergebnisse - "Sidhu, Alpa"

PubPharm (31)

1

Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish

enthalten in: Science advances | 2023

von Patterson, V. | Ullah, F. | Bryant, L. | +48

ErratumIn: Sci Adv. 2023 Nov 24;9(47):eadl5515. - PMID 38000037

2

Mosaicism in BRPF1-Related Neurodevelopmental Disorder : Report of Two Sisters and Literature Review

enthalten in: Case reports in genetics | 2023

von Bayanbold, K. | Younger, G. | Darbro, B. | +1

3

Prepregnancy exposure to dietary arsenic and congenital heart defects

enthalten in: Birth defects research | 2023

von Suhl, J. | Conway, K. | Rhoads, A. | +11

4

Erratum : Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3

enthalten in: HGG advances | 2022

von Nair, D. | Li, D. | Erdogan, H. | +19

ErratumFor: HGG Adv. 2021 Jan 21;2(2):100024. - PMID 35047834

5

Maternal cigarette smoking and alcohol consumption and congenital diaphragmatic hernia

enthalten in: Birth defects research | 2022

von Finn, J. | Suhl, J. | Kancherla, V. | +9

6

Pre-pregnancy exposure to arsenic in diet and non-cardiac birth defects

enthalten in: Public health nutrition | 2022

von Suhl, J. | Conway, K. | Rhoads, A. | +10

7

Co-occurrence of VHL and SDHA Pathogenic Variants : A Case Report

enthalten in: Frontiers in oncology | 2022

von Tung, M. | Chandra, B. | Dillahunt, K. | +3

8

Maternal cigarette smoking and alcohol consumption and congenital diaphragmatic hernia

enthalten in: Birth Defects Research | 2022

von Finn, J. | Suhl, J. | Kancherla, V. | +8

9

CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum

enthalten in: Clinical genetics | 2021

von Palmer, E. | Whitton, C. | Hashem, M. | +18

10

Interstitial duplication of 20q11.22q13.11 : A case report and review of literature

enthalten in: Molecular genetics & genomic medicine | 2021

von Goetzinger, L. | Starks, R. | Dillahunt, K. | +3