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  2. Median arcuate ligament syndrome - Wikipedia

    en.wikipedia.org/wiki/Median_arcuate_ligament...

    Median arcuate ligament syndrome is a diagnosis of exclusion. [ 2 ] [ 5 ] That is, the diagnosis of MALS is generally considered only after patients have undergone an extensive evaluation of their gastrointestinal tract including upper endoscopy , colonoscopy , and evaluation for gallbladder disease and gastroesophageal reflux disease (GERD).

  3. Hereditarianism - Wikipedia

    en.wikipedia.org/wiki/Hereditarianism

    Social scientist Barry Mehler defines hereditarianism as "the belief that a substantial part of both group and individual differences in human behavioral traits are caused by genetic differences". [1] Hereditarianism is sometimes used as a synonym for biological or genetic determinism, though some scholars distinguish the two terms. When ...

  4. Yes–no question - Wikipedia

    en.wikipedia.org/wiki/Yes–no_question

    In linguistics, a yesno question, also known as a binary question, a polar question, or a general question, [1] or closed-ended question is a question whose expected answer is one of two choices, one that provides an affirmative answer to the question versus one that provides a negative answer to the question.

  5. Yes, dyslexia can be genetic. But genes aren't the only ... - AOL

    www.aol.com/yes-dyslexia-genetic-genes-arent...

    There's no need to panic, though, Noorlander notes, "as early diagnosis and support through specialized teaching can make a big difference and help people with dyslexia manage their challenges and ...

  6. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]

  7. MAL (gene) - Wikipedia

    en.wikipedia.org/wiki/MAL_(gene)

    The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids.The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction.

  8. XX male syndrome - Wikipedia

    en.wikipedia.org/wiki/XX_male_syndrome

    XX male syndrome, also known as de la Chapelle syndrome, is a rare intersex condition in which an individual with a 46,XX karyotype develops a male phenotype. [2] Synonyms for XX male syndrome include 46,XX testicular difference of sex development (or 46,XX DSD) [3] [4] [5] [6]

  9. Primogeniture - Wikipedia

    en.wikipedia.org/wiki/Primogeniture

    The preference for males in most systems of primogeniture (and in other mechanisms of hereditary succession) comes mostly from the perceived nature of the tasks and role of the monarch: a monarch/prince (the latter means in Latin, chieftain) most usually was, first and foremost, a military leader, as in the Book of Numbers.