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Results: 1 to 20 of 177

Similar articles for PubMed (Select 9600734)

1.

Pacman dysplasia: report of two affected sibs.

Wilcox WR, Lucas BC, Loebel B, Bachman RP, Lachman RS, Rimoin DL.

Am J Med Genet. 1998 May 26;77(4):272-6.

PMID:
9600734
2.

A new autosomal recessive lethal chondrodystrophy with congenital hydrops.

Greenberg CR, Rimoin DL, Gruber HE, DeSa DJ, Reed M, Lachman RS.

Am J Med Genet. 1988 Mar;29(3):623-32.

PMID:
3377005
3.

First-trimester diagnosis of Blomstrand lethal osteochondrodysplasia.

den Hollander NS, van der Harten HJ, Vermeij-Keers C, Niermeijer MF, Wladimiroff JW.

Am J Med Genet. 1997 Dec 19;73(3):345-50.

PMID:
9415697
4.

A new lethal autosomal recessive skeletal dysplasia with associated dysmorphic features.

Morton JE, Kilby MD, Rushton I.

Clin Dysmorphol. 1998 Apr;7(2):109-14.

PMID:
9571280
5.

Clinical and radiographic delineation of odontochondrodysplasia.

Unger S, Antoniazzi F, Brugnara M, Alanay Y, Caglayan A, Lachlan K, Ikegawa S, Nishimura G, Zabel B, Spranger J, Superti-Furga A.

Am J Med Genet A. 2008 Mar 15;146A(6):770-8. doi: 10.1002/ajmg.a.32214.

PMID:
18241073
6.

Schneckenbecken dysplasia in fetus: report of four cases.

Lahmar-Boufaroua A, Yacoubi MT, Belaid L, Delezoide AL.

Fetal Diagn Ther. 2009;25(2):216-9. doi: 10.1159/000214860. Epub 2009 Apr 29.

PMID:
19407457
7.

Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs.

Brodie SG, Lachman RS, Jewell AF, Winkler CL, Nolasco L, Wilcox WR.

Am J Med Genet. 1998 Dec 4;80(4):423-8.

PMID:
9856576
8.

A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasia.

Borochowitz Z, Jones KL, Silbey R, Adomian G, Lachman R, Rimoin DL.

Am J Med Genet. 1986 Sep;25(1):47-59.

PMID:
3799723
9.

New epiphyseal stippling syndrome with osteoclastic hyperplasia.

Shohat M, Rimoin DL, Gruber HE, Lachman R.

Am J Med Genet. 1993 Mar 1;45(5):558-61.

PMID:
8456823
10.

Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.

Opitz JM, Spranger JW, Stöss HR, Pesch HJ, Azadeh B.

Am J Med Genet. 1987 Mar;26(3):583-90.

PMID:
3565474
11.

Fibrochondrogenesis: radiologic and histologic studies.

Eteson DJ, Adomian GE, Ornoy A, Koide T, Sugiura Y, Calabro A, Lungarotti S, Mastroiacovo P, Lachman RS, Rimoin DL.

Am J Med Genet. 1984 Oct;19(2):277-90.

PMID:
6507479
12.

Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.

Borochowitz Z, Langer LO Jr, Gruber HE, Lachman R, Katznelson MB, Rimoin DL.

Am J Med Genet. 1993 Feb 1;45(3):320-6.

PMID:
8434618
13.

Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder.

Chitayat D, Gruber H, Mullen BJ, Pauzner D, Costa T, Lachman R, Rimoin DL.

Am J Med Genet. 1993 Aug 15;47(2):272-7. Review.

PMID:
8213919
14.

Lethal osteosclerotic skeletal dysplasia with intracellular inclusion bodies.

Brodie SG, Lachman RS, McGovern MM, Mekikian PB, Wilcox WR.

Am J Med Genet. 1999 Apr 23;83(5):372-7.

PMID:
10232746
16.

Familial Blomstrand chondrodysplasia with advanced skeletal maturation: further delineation.

Loshkajian A, Roume J, Stanescu V, Delezoide AL, Stampf F, Maroteaux P.

Am J Med Genet. 1997 Aug 22;71(3):283-8. Review.

PMID:
9268097
17.
18.

Skeletal histopathology in fetuses with chondroectodermal dysplasia (Ellis-van Creveld syndrome).

Qureshi F, Jacques SM, Evans MI, Johnson MP, Isada NB, Yang SS.

Am J Med Genet. 1993 Feb 15;45(4):471-6.

PMID:
8465854
19.

Benign form of congenital angulation of long bones associated with shortening of soft tissues.

Nakamura K, Haga N, Manabe N, Iizuka T.

Clin Dysmorphol. 1998 Jan;7(1):1-10.

PMID:
9546823
20.

Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology.

Whitley CB, Langer LO Jr, Ophoven J, Gilbert EF, Gonzalez CH, Mammel M, Coleman M, Rosemberg S, Rodriques CJ, Sibley R, et al.

Am J Med Genet. 1984 Oct;19(2):265-75.

PMID:
6507478
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