-
2
-
-
0000042326
-
Healing of a fracture in an unusual case of congenital anomaly of the upper extremities
-
Gerold M. Healing of a fracture in an unusual case of congenital anomaly of the upper extremities. Zbl Chir 1959;84:831-4.
-
(1959)
Zbl Chir
, vol.84
, pp. 831-834
-
-
Gerold, M.1
-
4
-
-
0028244052
-
Phenotypic variability in the Baller-Gerold syndrome: Report of a mildly affected patient and review of the literature
-
Ramos Fuentes FJ, Nicholson L, Scott CI Jr. Phenotypic variability in the Baller-Gerold syndrome: Report of a mildly affected patient and review of the literature. Eur J Pediatr 1994;153:483-7.
-
(1994)
Eur J Pediatr
, vol.153
, pp. 483-487
-
-
Ramos Fuentes, F.J.1
Nicholson, L.2
Scott Jr., C.I.3
-
5
-
-
0016722568
-
An etiologic and nosologic overview of craniosynostosis syndromes
-
Cohen MM Jr. An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects 1975;11:137-89.
-
(1975)
Birth Defects
, vol.11
, pp. 137-189
-
-
Cohen Jr., M.M.1
-
9
-
-
0033555855
-
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: Further evidence for heterogeneity of Baller-Gerold syndrome
-
Gripp KW, Stolle CA, Celle L, McDonald-McGinn DM, Whitaker LA, Zackai EH. TWIST gene mutation in a patient with radial aplasia and craniosynostosis: Further evidence for heterogeneity of Baller-Gerold syndrome. Am J Med Genet 1999;82:170-6.
-
(1999)
Am J Med Genet
, vol.82
, pp. 170-176
-
-
Gripp, K.W.1
Stolle, C.A.2
Celle, L.3
McDonald-McGinn, D.M.4
Whitaker, L.A.5
Zackai, E.H.6
-
10
-
-
0141756130
-
Expanding the phenotypic spectrum of the Baller-Gerold syndrome
-
Temtamy SA, Aglan MS, Nemat A, Eid M. Expanding the phenotypic spectrum of the Baller-Gerold syndrome. Genet Couns 2003;14:299-312.
-
(2003)
Genet Couns
, vol.14
, pp. 299-312
-
-
Temtamy, S.A.1
Aglan, M.S.2
Nemat, A.3
Eid, M.4
-
11
-
-
0027459025
-
Further delineation of the Baller-Gerold syndrome
-
Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Further delineation of the Baller-Gerold syndrome. Am J Med Genet 1993;45:519-24.
-
(1993)
Am J Med Genet
, vol.45
, pp. 519-524
-
-
Lin, A.E.1
McPherson, E.2
Nwokoro, N.A.3
Clemens, M.4
Losken, H.W.5
Mulvihill, J.J.6
-
12
-
-
0025289046
-
The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome
-
Huson SM, Rodgers CS, Hall CM, Winter RM. The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome. J Med Genet 1990;27:371-5.
-
(1990)
J Med Genet
, vol.27
, pp. 371-375
-
-
Huson, S.M.1
Rodgers, C.S.2
Hall, C.M.3
Winter, R.M.4
-
13
-
-
0028265083
-
Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome
-
Farrell SA, Paes BA, Lewis ME. Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome. Am J Med Genet 1994;50:98-9.
-
(1994)
Am J Med Genet
, vol.50
, pp. 98-99
-
-
Farrell, S.A.1
Paes, B.A.2
Lewis, M.E.3
|