Novel mutation in MASP1 gene in a new family with 3MC syndrome.Clin Dysmorphol. 2019 Apr; 28(2):91-93.CD
Links
MeSH
Abdominal MusclesAbnormalities, MultipleAdultBlepharoptosisChildChild, PreschoolCraniofacial AbnormalitiesCraniosynostosesCryptorchidismDevelopmental DisabilitiesEye AbnormalitiesFamilyFemaleHeart Defects, CongenitalHip Dislocation, CongenitalHumansInfantMannose-Binding Protein-Associated Serine ProteasesPedigreeStrabismusSyndromeTurkey
Pub Type(s)
Case Reports
Journal Article
Language
eng
PubMed ID
30601195
Citation
Basdemirci, Muserref, et al. "Novel Mutation in MASP1 Gene in a New Family With 3MC Syndrome." Clinical Dysmorphology, vol. 28, no. 2, 2019, pp. 91-93.
Basdemirci M, Sen A, Ceylaner S. Novel mutation in MASP1 gene in a new family with 3MC syndrome. Clin Dysmorphol. 2019;28(2):91-93.
Basdemirci, M., Sen, A., & Ceylaner, S. (2019). Novel mutation in MASP1 gene in a new family with 3MC syndrome. Clinical Dysmorphology, 28(2), 91-93. https://doi.org/10.1097/MCD.0000000000000256
Basdemirci M, Sen A, Ceylaner S. Novel Mutation in MASP1 Gene in a New Family With 3MC Syndrome. Clin Dysmorphol. 2019;28(2):91-93. PubMed PMID: 30601195.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Novel mutation in MASP1 gene in a new family with 3MC syndrome.
AU - Basdemirci,Muserref,
AU - Sen,Askin,
AU - Ceylaner,Serdar,
PY - 2019/1/3/pubmed
PY - 2019/6/15/medline
PY - 2019/1/3/entrez
SP - 91
EP - 93
JF - Clinical dysmorphology
JO - Clin Dysmorphol
VL - 28
IS - 2
SN - 1473-5717
UR - https://www.unboundmedicine.com/medline/citation/30601195/Novel_mutation_in_MASP1_gene_in_a_new_family_with_3MC_syndrome_
L2 - https://doi.org/10.1097/MCD.0000000000000256
DB - PRIME
DP - Unbound Medicine
ER -
Latest evidence on COVID-19 from PubMed, WHO, CDC.
Visit free Relief Central.
Visit free Relief Central.
Try the Free App:
