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Congenital Anomalies
Latest Publications
TOTAL DOCUMENTS
1498
(FIVE YEARS 134)
H-INDEX
30
(FIVE YEARS 3)
Published By Wiley (Blackwell Publishing)
1741-5420, 0914-3505
Latest Documents
Most Cited Documents
Contributed Authors
Related Sources
Related Keywords
Latest Documents
Most Cited Documents
Contributed Authors
Related Sources
Related Keywords
Analysis of triptan use during pregnancy in Japan: A case series
Congenital Anomalies
◽
10.1111/cga.12456
◽
2022
◽
Author(s):
Yuko Yamaguchi
◽
Takahiro Yamada
◽
Mikako Goto
◽
Hidenori Kawasaki
◽
Takahito Wada
◽
...
Keyword(s):
Case Series
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Issue Information
Congenital Anomalies
◽
10.1111/cga.12423
◽
2022
◽
Vol 62
(1)
◽
pp. 1-3
Download Full-text
The Japanese Teratology Society 61st Annual Meeting
Congenital Anomalies
◽
10.1111/cga.12453
◽
2022
◽
Vol 62
(1)
◽
Keyword(s):
Annual Meeting
Download Full-text
Announcement
Congenital Anomalies
◽
10.1111/cga.12455
◽
2022
◽
Vol 62
(1)
◽
pp. 49-49
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Potential role of viral infections in miscarriage and insights into the underlying molecular mechanisms
Congenital Anomalies
◽
10.1111/cga.12458
◽
2021
◽
Author(s):
Zahra Heydarifard
◽
Sevrin Zadheidar
◽
Jila Yavarian
◽
Somayeh Shatizadeh Malekshahi
◽
Shirin Kalantari
◽
...
Keyword(s):
Molecular Mechanisms
◽
Potential Role
◽
Viral Infections
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Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations
Congenital Anomalies
◽
10.1111/cga.12457
◽
2021
◽
Author(s):
Rasha Elhossini
◽
Mohamed S. Abdel‐Hamid
◽
Engy Ashaat
◽
Ghada A. Otaify
◽
Heba Dawoud
◽
...
Keyword(s):
Focal Dermal Hypoplasia
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Cohesinopathy presenting with microtia, facial palsy and hearing loss caused by STAG1 pathogenic variant
Congenital Anomalies
◽
10.1111/cga.12454
◽
2021
◽
Author(s):
Michinori Funato
◽
Tomoko Uehara
◽
Yuuki Okada
◽
Hideo Kaneko
◽
Kenjiro Kosaki
Keyword(s):
Hearing Loss
◽
Facial Palsy
◽
Pathogenic Variant
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Involvement of homeobox transcription factor Mohawk in palatogenesis
Congenital Anomalies
◽
10.1111/cga.12451
◽
2021
◽
Author(s):
Yuka Adachi
◽
Aina Higuchi
◽
Eri Wakai
◽
Takashi Shiromizu
◽
Junko Koiwa
◽
...
Keyword(s):
Transcription Factor
◽
Homeobox Transcription Factor
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Identification of a novel mutant allele of LIM homeobox transcription factor 1 alpha ( dreher ) in mice
Congenital Anomalies
◽
10.1111/cga.12450
◽
2021
◽
Author(s):
Jun‐ichi Suto
Keyword(s):
Transcription Factor
◽
Mutant Allele
◽
Homeobox Transcription Factor
◽
Transcription Factor 1
Download Full-text
Periconceptional folic acid intake and disturbing factors: A single‐center study in Japan
Congenital Anomalies
◽
10.1111/cga.12449
◽
2021
◽
Author(s):
Shunsuke Kamura
◽
Aiko Sasaki
◽
Kohei Ogawa
◽
Kiyoko Kato
◽
Haruhiko Sago
Keyword(s):
Folic Acid
◽
Single Center
◽
Folic Acid Intake
◽
Acid Intake
◽
Single Center Study
◽
Center Study
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