Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Saabti, H."'
Publikováno v:
Ophthalmic Genetics. 21:211-216
We describe a child with global developmental delay, prominent metopic suture, trigonocephaly, and cryptorchidism whose symptoms resemble the well-known 9p deletion syndrome or 9p monosomy. We also noted congenital hydrocephalus, oculocutaneous albin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c31d92bdfa0c25d50b1cc11531a922e5
https://doi.org/10.1076/1381-6810(200012)2141-hft211
https://doi.org/10.1076/1381-6810(200012)2141-hft211
Autor:
Hale, Andrew T.1 (AUTHOR) andrewthale@uabmc.edu, Boudreau, Hunter1 (AUTHOR), Devulapalli, Rishi2 (AUTHOR), Duy, Phan Q.3 (AUTHOR), Atchley, Travis J.1 (AUTHOR), Dewan, Michael C.4 (AUTHOR), Goolam, Mubeen5 (AUTHOR), Fieggen, Graham5,6 (AUTHOR), Spader, Heather L.3 (AUTHOR), Smith, Anastasia A.7 (AUTHOR), Blount, Jeffrey P.7 (AUTHOR), Johnston, James M.7 (AUTHOR), Rocque, Brandon G.7 (AUTHOR), Rozzelle, Curtis J.7 (AUTHOR), Chong, Zechen8 (AUTHOR), Strahle, Jennifer M.9 (AUTHOR), Schiff, Steven J.10 (AUTHOR), Kahle, Kristopher T.11 (AUTHOR)
Publikováno v:
Fluids & Barriers of the CNS. 3/4/2024, Vol. 21 Issue 1, p1-135. 135p.
Publikováno v:
Ophthalmic Genetics; Dec2000, Vol. 21 Issue 4, p211-216, 6p
Autor:
Leung, Kai Ching Peter1 (AUTHOR) heyays@gmail.com, Ko, Tak Chuen Simon1 (AUTHOR)
Publikováno v:
Ophthalmic Genetics. Aug2020, Vol. 41 Issue 4, p373-376. 4p.
Publikováno v:
Ophthalmic Genetics. Dec2000, Vol. 21 Issue 4, p259-260. 2p.