Results 121 to 130 of about 322,265 (340)

Case Series of Nizon‐Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid–Triploid Mosaicism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nizon‐Isidor syndrome is a rare disorder caused by heterozygous variants in MED12L, with only eight documented cases in the literature. Here, we present three additional cases of this syndrome. Proband 1 was a 7‐year‐old female who presented with developmental delay, right‐leg hemihypertrophy, laryngeal cleft, esotropia, abnormal skin ...
Russell Stewart   +336 more
wiley   +1 more source

Descriptive Analysis of Sexual Assault Nurse Examinations in Fairbanks: 2005-2006 [PDF]

open access: yes, 2007
This project examined the characteristics of 144 sexual assault victimizations recorded by sexual assault nurse examiners in Fairbanks, Alaska in 2005 and 2006. The report documents the demographic characteristics of patients, pre-assault characteristics,
Fairbanks Memorial Hospital   +3 more
core  

A prepubic urethrostomy in a bitch after resection of the vagina and the distal part of the urethra [PDF]

open access: bronze, 2006
Marije Risselada   +5 more
openalex   +1 more source

A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss‐of‐Function of DMRT2

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Spondylocostal dysostosis (SCDO) is a rare genetic disorder characterized by abnormal development of the axial skeleton, resulting in malformations of the vertebrae and ribs that often impair lung development and lead to significant respiratory morbidity.
Jonathan Rips   +8 more
wiley   +1 more source

Spartan Daily, November 29, 2018 [PDF]

open access: yes, 2018
Volume 151, Issue 41https://scholarworks.sjsu.edu/spartan_daily_2018/1083/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core   +1 more source

Persistent urogenital sinus with bladder agenesis and absence of vagina [PDF]

open access: bronze, 2003
Antonio Savanelli   +5 more
openalex   +1 more source

A clinicopathological study of malignant melanoma with special reference to atypical presentation

open access: yesIndian Journal of Pathology and Microbiology, 2008
Malignant melanoma is a tumor of melanocytic origin. Lymphatic and hematogenous metastases are common in this condition. Retrospective analysis was performed in 16 consecutive cases diagnosed histopathologically as malignant melanoma at the pathology ...
Mukhopadhyay Subhalakshmi   +3 more
doaj  

Leiomyoma of the vagina that caused cyclic urinary retention [PDF]

open access: bronze, 2007
Su Jeong Park   +5 more
openalex   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss   +8 more
wiley   +1 more source

A systematic review of transgender male rodent model methodology

open access: yesAnimal Models and Experimental Medicine, EarlyView.
Summary of successful transgender male rodent model methods. Testosterone enanthate or cypionate injected SC or IM once per week at 18 mg/kg in mice or 3 mg/kg in rats should effectively match naive male testosterone levels of their respective species.
Kai Robertson   +4 more
wiley   +1 more source

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