Molecular Breakpoint Cloning and Gene Expression Studies of a Novel Translocation T(4;15)(q27;q11.2) Associated With Prader-Willi Syndrome

BMC Medical Genetics - United Kingdom
doi 10.1186/1471-2350-6-18
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Prader-Willi Syndrome

2020English

Prader-Willi Syndrome

English

PO-0366 Prader-Willi Syndrome: 3 Cases Studies

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
2014English

A Clinical, Cytogenetic, and Molecular Study of 40 Adults With the Prader-Willi Syndrome.

Journal of Medical Genetics
Genetics
1995English

Birth Seasonality Studies in a Large Prader-Willi Syndrome Cohort

American Journal of Medical Genetics, Part A
Genetics
2019English

Prader-Willi Syndrome in a Child With XYY

Journal of Human Genetics
Genetics
1999English

Prader-Willi Syndrome Association UK

2018English

Physical Exercise and Prader-Willi Syndrome: A Systematic Review

Clinical Endocrinology
EndocrinologyMetabolismDiabetes
2019English

Nutritient Intake of Young Children With Prader–Willi Syndrome

Food and Nutrition Research
NutritionDieteticsPublic HealthFood ScienceEnvironmentalOccupational Health
2010English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy