Mundlos S - Search Results

1

Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.

Kant SG, Polinkovsky A, Mundlos S, Zabel B, Thomeer RT, Zonderland HM, Shih L, van Haeringen A, Warman ML. Kant SG, et al. Among authors: mundlos s. Am J Hum Genet. 1998 Jul;63(1):155-62. doi: 10.1086/301917. Am J Hum Genet. 1998. PMID: 9634515 Free PMC article.

2

Distribution of osteonectin mRNA and protein during human embryonic and fetal development.

Mundlos S, Schwahn B, Reichert T, Zabel B. Mundlos S, et al. J Histochem Cytochem. 1992 Feb;40(2):283-91. doi: 10.1177/40.2.1552170. J Histochem Cytochem. 1992. PMID: 1552170

3

Distribution of cartilage proteoglycan (aggrecan) core protein and link protein gene expression during human skeletal development.

Mundlos S, Meyer R, Yamada Y, Zabel B. Mundlos S, et al. Matrix. 1991 Nov;11(5):339-46. doi: 10.1016/s0934-8832(11)80205-2. Matrix. 1991. PMID: 1725805

4

Distribution of type I and type II collagen gene expression during the development of human long bones.

Mundlos S, Engel H, Michel-Behnke I, Zabel B. Mundlos S, et al. Bone. 1990;11(4):275-9. doi: 10.1016/8756-3282(90)90080-i. Bone. 1990. PMID: 2242293

5

Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasia.

Spranger J, Menger H, Mundlos S, Winterpacht A, Zabel B. Spranger J, et al. Among authors: mundlos s. Pediatr Radiol. 1994;24(6):431-5. doi: 10.1007/BF02011911. Pediatr Radiol. 1994. PMID: 7700721

6

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.

Mundlos S, Mulliken JB, Abramson DL, Warman ML, Knoll JH, Olsen BR. Mundlos S, et al. Hum Mol Genet. 1995 Jan;4(1):71-5. doi: 10.1093/hmg/4.1.71. Hum Mol Genet. 1995. PMID: 7711736

7

Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasia.

Winterpacht A, Schwarze U, Mundlos S, Menger H, Spranger J, Zabel B. Winterpacht A, et al. Among authors: mundlos s. Hum Mol Genet. 1994 Oct;3(10):1891-3. doi: 10.1093/hmg/3.10.1891. Hum Mol Genet. 1994. PMID: 7849719 No abstract available.

8

Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutation.

Winterpacht A, Hilbert M, Schwarze U, Mundlos S, Spranger J, Zabel B. Winterpacht A, et al. Among authors: mundlos s. Hum Mutat. 1994;4(4):257-62. doi: 10.1002/humu.1380040405. Hum Mutat. 1994. PMID: 7866404

9

Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect.

Winterpacht A, Hilbert M, Schwarze U, Mundlos S, Spranger J, Zabel BU. Winterpacht A, et al. Among authors: mundlos s. Nat Genet. 1993 Apr;3(4):323-6. doi: 10.1038/ng0493-323. Nat Genet. 1993. PMID: 7981752

10

Developmental expression of human cartilage matrix protein.

Mundlos S, Zabel B. Mundlos S, et al. Dev Dyn. 1994 Mar;199(3):241-52. doi: 10.1002/aja.1001990308. Dev Dyn. 1994. PMID: 8018988 Free article.

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