Marfan syndrome: a mystery solved.

ανά Tsipouras, P
Έκδοση 1992

A workshop on Marfan syndrome, 10 June 1989, Farmington, CT, USA.

ανά Tsipouras, P
Έκδοση 1990

Marfan syndrome: light at the end of the tunnel?

ανά Tsipouras, P
Έκδοση 1990

Genetic disorders of collagen.

ανά Tsipouras, P, Ramirez, F
Έκδοση 1987

Linkage disequilibrium between two restriction sites in the COL2A1 gene.

ανά Schwartz, R C, Sarfarazi, M, Tsipouras, P
Έκδοση 1990

Lack of linkage disequilibrium between two common restriction sites associated with the COLIA2 gene.

ανά Halloran-Blanton, S, Schwartz, R C, Tsipouras, P
Έκδοση 1989

Two RFLPs in the 5' end of the human osteonectin (ON) gene.

ανά Schwartz, R C, Young, M F, Tsipouras, P
Έκδοση 1988

Osteogenesis imperfecta type IV. Biochemical confirmation of genetic linkage to the pro alpha 2(I) gene of type I collagen.

ανά Wenstrup, R J, Tsipouras, P, Byers, P H
Έκδοση 1986

Possible genetic heterogeneity in hypochondroplasia.

ανά Stoilov, I, Kilpatrick, M W, Tsipouras, P, Costa, T
Έκδοση 1995

An RFLP in the gene for the human pro-alpha 2 chain of type V collagen (COL5A2).

ανά Schwartz, R C, Liddell, A, Ramirez, F, Tsipouras, P
Έκδοση 1988

Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta.

ανά Falk, C T, Schwartz, R C, Ramirez, F, Tsipouras, P
Έκδοση 1986

Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.

ανά Tsipouras, P, Sarfarazi, M, Devi, A, Weiffenbach, B, Boxer, M
Έκδοση 1991

Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesi...

ανά Tsipouras, P, Myers, J C, Ramirez, F, Prockop, D J
Έκδοση 1983

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

ανά Sher, C, Ramesar, R, Martell, R, Learmonth, I, Tsipouras, P, Beighton, P
Έκδοση 1991

Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe.

ανά Tsipouras, P, Schwartz, R C, Goldberg, J D, Berkowitz, R L, Ramirez, F
Έκδοση 1987

Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI).

ανά Anderson, I J, Goldberg, R B, Marion, R W, Upholt, W B, Tsipouras, P
Έκδοση 1990

Perinatal lethal osteogenesis imperfecta (OI type II): a biochemically heterogeneous disorder usually due to new mutations in the genes for type I collagen.

ανά Byers, P H, Tsipouras, P, Bonadio, J F, Starman, B J, Schwartz, R C
Έκδοση 1988

Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndrome.

ανά Fryer, A E, Upadhyaya, M, Littler, M, Bacon, P, Watkins, D, Tsipouras, P, Harper, P S
Έκδοση 1990

Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfecta.

ανά Tsipouras, P, Børresen, A L, Dickson, L A, Berg, K, Prockop, D J, Ramirez, F
Έκδοση 1984

Linkage analysis in Marfan syndrome.

ανά Schwartz, R C, Blanton, S H, Hyde, C A, Sottile, T R, Hudgins, L, Sarfarazi, M, Tsipouras, P
Έκδοση 1990