Zobrazeno 1 - 10
of 955
pro vyhledávání: '"S. M. Darling"'
Publikováno v:
Clinical genetics, 29(3), 251-257. Wiley-Blackwell
A newborn girl, homozygous for a balanced Y/22 chromosome translocation is described. This unique karyotype was detected during prenatal chromosome studies in the first pregnancy of a 26-year-old woman. Amniocentesis was performed because of clinical
Autor:
Chaturvedi, Ruchi Dubey1 ruchi.chaturvedi@jaihindcollege.edu.in, Shinde, Freyana1, Khatri, Palak1, Sandesara, Pankti1, Jadhav, Swarali1, Gami, Mayuri1
Publikováno v:
Indian Journal of Positive Psychology. Sep2024, Vol. 15 Issue 3, p360-363. 4p.
Autor:
Yuping Wei1,2,3 (AUTHOR), Ziyang Liu1,2 (AUTHOR), Man Zhang, Man Zhang2,4 (AUTHOR), Xingyan Zhu1,2 (AUTHOR), Qiuhong Niu1,2 (AUTHOR) fuziannwei@163.com
Publikováno v:
Molecules. Jul2024, Vol. 29 Issue 13, p1-15. 15p. 6 Graphs.
Autor:
de Jong, Rineke1 (AUTHOR), Nuiten, Wout1 (AUTHOR), ter Heide, Albertjan1 (AUTHOR), Hamstra, Wilfred1 (AUTHOR), Vreman, Sandra1 (AUTHOR), Oreshkova, Nadia1 (AUTHOR), Wiese, Katrin E.1 (AUTHOR), Gerhards, Nora M.1 (AUTHOR) nora.gerhards@wur.nl
Publikováno v:
Viruses (1999-4915). Jul2024, Vol. 16 Issue 7, p1022. 13p.
Publikováno v:
The International journal of developmental biology. 41(5)
The semidominant mouse mutation hypodactyly (Hd), caused by a deletion within the Hoxa13 gene, results in reduced digits; heterozygotes lack digit I in the hindlimb and homozygotes have only one digit on each limb. We investigated expression of Shh a
Autor:
Peng, Huimin1 (AUTHOR), Jing, Longjun1 (AUTHOR), Liu, Yang2 (AUTHOR), Tang, Yiwei1 (AUTHOR), Wang, Huilin3 (AUTHOR)
Publikováno v:
Social Behavior & Personality: an international journal. Jun2024, Vol. 52 Issue 6, p1-10. 10p.
Autor:
Gandini, Andi Lis Arming1,2 anwar_envi@yahoo.com, Salmah, A. Ummu2, Stang2, Arsin, A. Arsunan2, Mallongi, Anwar2
Publikováno v:
Pharmacognosy Journal. May/Jun2024, Vol. 16 Issue 3, p682-686. 5p.
Publikováno v:
Developmental genetics. 19(1)
The limb defect in the mouse Hypodactyly (Hd) affects only the distal structures. Heterozygotes (Hd/+) lack all or part of the distal phalanx and the terminal claw of digit on the hindlimbs; mice homozygous (Hd/Hd) for the mutation have just one digi
Autor:
Paul S. Burgoyne, Á. Rattigan, Blanche Capel, S. M. Darling, Shantha K. Mahadevaiah, S. J. Conway
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 5(4)
There is evidence from Y Chromosome (Chr) deletion mapping that there is a gene on the long arm of the mouse Y Chr that is needed for the normal development of the sperm head. Since mice with partial Y long arm deletions show incomplete penetrance of
Autor:
Villarejo, Sonia1, Garcia, Oscar F.1 oscar.f.garcia@uv.es, Alcaide, Marta1, Villarreal, Maria E.2, Garcia, Fernando1
Publikováno v:
Psychosocial Intervention. Jan2024, Vol. 33 Issue 1, p15-27. 13p.