Suchergebnisse - "Holoprosencephaly"

PubPharm (493)

91

The Role of Sonic Hedgehog in Human Holoprosencephaly and Short-Rib Polydactyly Syndromes

in: International Journal of Molecular Sciences | 2021

von Christine K. C. Loo | Michael A. Pearen | Grant A. Ramm

92

in: International Journal of Molecular Sciences | 2021

von Laura Castilla-Vallmanya | Semra Gürsoy | Özlem Giray-Bozkaya | +8

93

Solitary median maxillary central incisor: A case report with 3-year follow-up and literature review

in: Contemporary Clinical Dentistry | 2021

von Triveni Mohan Nalawade | Rachappa M Mallikarjuna | H P Suma Sogi | +2

94

Case Report: An Infant With Kabuki Syndrome, Alobar Holoprosencephaly and Truncus Arteriosus: A Case for Whole Exome Sequencing in Neonates With Congenital Anomalies

in: Frontiers in Genetics | 2021

von Rishika P. Sakaria | Rishika P. Sakaria | Parul G. Zaveri | +8

95

Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta

in: Taiwanese Journal of Obstetrics & Gynecology | 2021

von Chih-Ping Chen | Chao-Yun Wu | Schu-Rern Chern | +4

96

Preterm infant with diprosopus and holoprosencephaly

in: Clinical Case Reports | 2021

von Nitya M. Nair | Daniel T. Swarr | Maria E. Barnes‐Davis

97

Identifying environmental risk factors and gene-environment interactions in holoprosencephaly

enthalten in: Birth defects research | 2021

von Addissie, Y. | Troia, A. | Wong, Z. | +6

98

Functional analysis of Sonic Hedgehog variants associated with holoprosencephaly in humans using a CRISPR/Cas9 zebrafish model

enthalten in: Human mutation | 2020

von Hong, S. | Hu, P. | Jang, J. | +5

99

The hedgehog co-receptor BOC differentially regulates SHH signaling during craniofacial development

enthalten in: Development (Cambridge, England) | 2020

von Echevarría-Andino, M. | Allen, B.

100

Rare hypomorphic human variation in the heptahelical domain of SMO contributes to holoprosencephaly phenotypes

enthalten in: Human mutation | 2020

von Nagai-Tanima, M. | Hong, S. | Hu, P. | +4