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Autor:
مریم موتمر1 maryam.motamer@gmail.com, مریم کدیور2
Publikováno v:
Tehran University Medical Journal. May2023, Vol. 81 Issue 2, p110-119. 10p.
Autor:
Barnard, Noel
Publikováno v:
American Anthropologist, 1968 Apr 01. 70(2), 404-405.
Externí odkaz:
https://www.jstor.org/stable/671178
Autor:
Chungsu Hwang1, Sojeong Lee1, Ahrong Kim1, Young-Geum Kim1, Sang-Jeong Ahn1, Do Youn Park1 pdy220@pusan.ac.kr
Publikováno v:
Cancer Research & Treatment. 2016, Vol. 48 Issue 4, p1222-1228. 7p.
Autor:
Noel Barnard
Publikováno v:
American Anthropologist. 70:404-405
Publikováno v:
Journal of Obstetrics and Gynaecology Canada. 39:886-889
Background Down syndrome is a chromosomal abnormality characterized by an additional acrocentric chromosome, resulting in an aneuploid number of 47 chromosomes (trisomy 21). Fetal face phenotype of Down syndrome is typical in the second trimester and
Autor:
Courdier, Cécile, Boudjarane, John, Malan, Valérie, Muti, Christine, Sperelakis‐Beedham, Brian, Odent, Sylvie, Jaillard, Sylvie, Quelin, Chloé, Le Caignec, Cédric, Patat, Olivier, Dubucs, Charlotte, Julia, Sophie, Schluth‐Bolard, Caroline, Goumy, Carole, Redon, Sylvia, Gaillard, Jean‐Baptiste, Huynh, Minh Tuan, Dupont, Céline, Tabet, Anne‐Claude, Cogan, Guillaume
Publikováno v:
Prenatal Diagnosis; Jun2023, Vol. 43 Issue 6, p734-745, 12p
Publikováno v:
Cold Spring Harbor Molecular Case Studies
Beckwith–Wiedemann syndrome (BWS) is a rare overgrowth disorder caused by epigenetic alterations on Chromosome 11p15.5. Most molecular changes are sporadic and are thought to occur in a mosaic pattern. Thereby, the distribution of affected cells di
Publikováno v:
Pan African Medical Journal. Jan-Apr2019, Vol. 32, p1-10. 10p.
Autor:
Shang, Yu, Ma, Yao, Tang, Sheng, Chen, Xing, Feng, Helong, Li, Li, Wang, Hongcai, Zeng, Zhe, Yao, Lun, Zhang, Tengfei, Zeng, Chi, Luo, Qingping, Wen, Guoyuan
Publikováno v:
Vaccines; Dec2023, Vol. 11 Issue 12, p1768, 12p