Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
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Involvement of Fibroblast Growth Factors and Their Receptors in Epididymo-Testicular Descent and MaldescentThe genetic landscape and clinical implications of vertebral anomalies in VACTERL associationTargeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.Molecular mechanisms of cryptorchidism development: update of the database, disease comorbidity, and initiative for standardization of reporting in scientific literature.Genetic Syndromes Affecting Kidney Development.Genetic Testing in a Cohort of Complex Esophageal Atresia.Inhibin B in healthy and cryptorchid boys
P2860
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P2860
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
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name
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@en
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@nl
type
label
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@en
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@nl
altLabel
HeterozygousFGF8mutations in p ...... eatures without limb anomalies
@en
prefLabel
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@en
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@nl
P2093
P2860
P356
P1476
Heterozygous FGF8 mutations in ...... atures without limb anomalies.
@en
P2093
Alina C Hilger
Anke Rißmann
Christina Kujath
Claudia Zeidler
Dominik Schmidt
Eberhard Schmiedeke
Ekkehart Jenetzky
Enrika Bartels
Gabriel C Dworschak
Greta Große
P2860
P304
P356
10.1002/BDRA.23278
P577
2014-08-08T00:00:00Z