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searching for X-linked recessive inheritance 13 found (36 total)

alternate case: x-linked recessive inheritance

Alopecia contractures dwarfism mental retardation syndrome (174 words) [view diff] exact match in snippet view article find links to article

between cases reported by year 2000 seem to suggest autosomal or x-linked recessive inheritance or possibly a dominant mutation caused by mosaicism as causes
Warkany syndrome 1 (215 words) [view diff] exact match in snippet view article find links to article
no longer diagnosed. The family history was consistent with X-linked recessive inheritance of intrauterine growth retardation and small head size, but
Glycogen storage disease type IX (610 words) [view diff] exact match in snippet view article find links to article
in. Glycogen storage disease type IX can be inherited via: X-linked recessive inheritance due to mutations at either PHKA1 or the PHKA2 (most common)
Aarskog–Scott syndrome (1,037 words) [view diff] exact match in snippet view article find links to article
X-linked recessive inheritance.
Boomerang dysplasia (814 words) [view diff] exact match in snippet view article find links to article
overlap. Early journal reports of boomerang dysplasia suggested X-linked recessive inheritance, based on observation and family history. It was later discovered
Mucopolysaccharidosis (2,927 words) [view diff] exact match in snippet view article find links to article
Hunter syndrome has two clinical subtypes and (since it shows X-linked recessive inheritance) is the only one of the mucopolysaccharidoses in which the mother
Holoprosencephaly (1,433 words) [view diff] exact match in snippet view article find links to article
HPE is inherited (autosomal dominant as well as autosomal or X-linked recessive inheritance).[citation needed] Features consistent with familial transmission
Allan–Herndon–Dudley syndrome (919 words) [view diff] exact match in snippet view article find links to article
cannot pass X-linked traits to their sons.[citation needed] In X-linked recessive inheritance, a female with one altered copy of the gene in each cell is
Monochromacy (1,978 words) [view diff] exact match in snippet view article find links to article
1987.01060080057028. PMID 2888453. Spivey, B E (1965). "The X-linked recessive inheritance of atypical monochromatism". Arch. Ophthalmol. 74 (3): 327–333
Say–Meyer syndrome (1,010 words) [view diff] exact match in snippet view article find links to article
3 males who were all related. Each male was found to have a X-linked recessive inheritance. The oldest one was found to be mentally retarded while the
Blue cone monochromacy (3,433 words) [view diff] exact match in snippet view article find links to article
1126/science.2788922. PMID 2788922. Spivey, B E (1965). "The X-linked recessive inheritance of atypical monochromatism". Arch. Ophthalmol. 74 (3): 327–333
Color blindness (9,142 words) [view diff] exact match in snippet view article find links to article
X-linked recessive inheritance
Xp11.2 duplication (3,253 words) [view diff] exact match in snippet view article find links to article
familial. Familial carriers of small duplication (<1 Mb) show X-linked recessive inheritance. All other affected individuals with larger duplication present