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6. 50 Years Ago in TheJournalofPediatrics: The Newborn Electrocardiogram. Solevåg AL; Saugstad OD J Pediatr; 2021 Jan; 228():52. PubMed ID: 33342502 [No Abstract] [Full Text] [Related]
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12. Arthrogryposis multiplex congenita. Report of two cases of a radicular type with familial incidence. Peña CE; Miller F; Budzilovich GN; Feigin I Neurology; 1968 Sep; 18(9):926-30. PubMed ID: 4176659 [No Abstract] [Full Text] [Related]
13. First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report. Kamal NM; Alzeky AM; Omair MR; Attar RA; Alotaibi AM; Safar A; Alosaimi NS; Abosabie SAS Ital J Pediatr; 2022 Jun; 48(1):107. PubMed ID: 35739559 [TBL] [Abstract][Full Text] [Related]
14. Non-lethal arthrogryposis multiplex congenita presenting with cystic hygroma at 13 weeks gestational age. Scott H; Hunter A; Bédard B Prenat Diagn; 1999 Oct; 19(10):966-71. PubMed ID: 10521824 [TBL] [Abstract][Full Text] [Related]
15. Arthrogryposis multiplex congenita (amyoplasia): an orthopaedic perspective. Bevan WP; Hall JG; Bamshad M; Staheli LT; Jaffe KM; Song K J Pediatr Orthop; 2007; 27(5):594-600. PubMed ID: 17585274 [No Abstract] [Full Text] [Related]
16. Development of a research platform for children with arthrogryposis multiplex congenita: study protocol for a pilot registry. Dahan-Oliel N; Bedard T; Darsaklis VB; Hall JG; van Bosse HJP; Hamdy RC BMJ Open; 2018 Jun; 8(6):e021377. PubMed ID: 29961027 [TBL] [Abstract][Full Text] [Related]
17. Earliest evidence for arthrogryposis multiplex congenita or Larsen syndrome? Anderson T Am J Med Genet; 1997 Aug; 71(2):127-9. PubMed ID: 9217208 [TBL] [Abstract][Full Text] [Related]
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20. Detection of mosaic isochromosome 20q in amniotic fluid in a pregnancy with fetal arthrogryposis multiplex congenita and normal karyotype in fetal blood and postnatal samples of placenta, skin, and liver. Chen CP Prenat Diagn; 2003 Jan; 23(1):85-7. PubMed ID: 12533820 [No Abstract] [Full Text] [Related] [Next] [New Search]