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Journal Abstract Search
438 related items for PubMed ID: 37023242
1. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Cheng S, Lo IFM, Luk HM. ; 1993. PubMed ID: 37023242 [Abstract] [Full Text] [Related]
2. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Mehta PA, Ebens C. ; 1993. PubMed ID: 20301575 [Abstract] [Full Text] [Related]
3. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Nunes ME. ; 1993. PubMed ID: 20301329 [Abstract] [Full Text] [Related]
4. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Roberts AE. ; 1993. PubMed ID: 20301303 [Abstract] [Full Text] [Related]
5. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, McCray BA, Schindler A, Hoover-Fong JE, Sumner CJ. ; 1993. PubMed ID: 24830047 [Abstract] [Full Text] [Related]
6. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Loeys BL, Dietz HC. ; 1993. PubMed ID: 20301312 [Abstract] [Full Text] [Related]
7. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Shuman C, Kalish JM, Weksberg R. ; 1993. PubMed ID: 20301568 [Abstract] [Full Text] [Related]
8. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Phelan K, Rogers RC, Boccuto L. ; 1993. PubMed ID: 20301377 [Abstract] [Full Text] [Related]
9. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Dietz H. ; 1993. PubMed ID: 20301510 [Abstract] [Full Text] [Related]
10. Report of a novel variant in the FAM111A gene in a fetus with multiple anomalies including gracile bones, hypoplastic spleen, and hypomineralized skull. Müller R, Steffensen T, Krstić N, Cain MA. Am J Med Genet A; 2021 Jun; 185(6):1903-1907. PubMed ID: 33750016 [Abstract] [Full Text] [Related]
12. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lin AE, Brunetti-Pierri N, Lindsay ME, Schimmenti LA, Starr LJ. ; 1993 Jun. PubMed ID: 28406602 [Abstract] [Full Text] [Related]
13. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Marzin P, Cormier-Daire V. ; 1993 Jun. PubMed ID: 20301776 [Abstract] [Full Text] [Related]
14. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Nelson A, Myers K. ; 1993 Jun. PubMed ID: 20301722 [Abstract] [Full Text] [Related]
15. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Priolo M. ; 1993 Jun. PubMed ID: 39083629 [Abstract] [Full Text] [Related]
16. Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2. Eren E, Tezcan Ünlü H, Ceylaner S, Tarım Ö. J Clin Res Pediatr Endocrinol; 2023 Feb 27; 15(1):97-102. PubMed ID: 34382758 [Abstract] [Full Text] [Related]
17. FAM111A mutations result in hypoparathyroidism and impaired skeletal development. Unger S, Górna MW, Le Béchec A, Do Vale-Pereira S, Bedeschi MF, Geiberger S, Grigelioniene G, Horemuzova E, Lalatta F, Lausch E, Magnani C, Nampoothiri S, Nishimura G, Petrella D, Rojas-Ringeling F, Utsunomiya A, Zabel B, Pradervand S, Harshman K, Campos-Xavier B, Bonafé L, Superti-Furga G, Stevenson B, Superti-Furga A. Am J Hum Genet; 2013 Jun 06; 92(6):990-5. PubMed ID: 23684011 [Abstract] [Full Text] [Related]
18. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Laurent MR, Harvengt P, Mortier GR, Böckenhauer D. ; 1993 Jun 06. PubMed ID: 22319799 [Abstract] [Full Text] [Related]
19. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Valverde de Morales HG, Wang HL, Garber K, Corces V, Li H. ; 1993 Jun 06. PubMed ID: 38662876 [Abstract] [Full Text] [Related]
20. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Sun A, Wang R. ; 1993 Jun 06. PubMed ID: 38190471 [Abstract] [Full Text] [Related] Page: [Next] [New Search]