Of mice and men: heritable skeletal disorders

about

Chicken collagen X regulatory sequences restrict transgene expression to hypertrophic cartilage in mice.Growth plate compressions and altered hematopoiesis in collagen X null mice.Molecular basis for skeletal variation: insights from developmental genetic studies in mice.

P2860

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Of mice and men: heritable skeletal disorders

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1994 nî lūn-bûn

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1994年の論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年论文

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1994年论文

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1994年论文

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name

Of mice and men: heritable skeletal disorders

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Of mice and men: heritable skeletal disorders

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Of mice and men: heritable skeletal disorders

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Of mice and men: heritable skeletal disorders

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Of mice and men: heritable skeletal disorders

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Of mice and men: heritable skeletal disorders

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P1476

Of mice and men: heritable skeletal disorders

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P2093

B R Olsen

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M L Warman

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O Jacenko

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P2860

Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid

Transgenic mouse model of the mild dominant form of osteogenesis imperfecta

Targeted disruption of the mouse transforming growth factor-beta 1 gene results in multifocal inflammatory disease

Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1

Mutations in collagen genes: causes of rare and some common diseases in humans

The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF beta superfamily

Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice

A linkage map spanning the locus for diastrophic dysplasia (DTD).

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163-168

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scholarly article

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English

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1994-02-01T00:00:00Z

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8304335

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1918165

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Of mice and men: heritable skeletal disorders

about

P2860

P2860

Of mice and men: heritable skeletal disorders

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P1433

P1476

P2093

P2860

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P304

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P932