Detalhe da pesquisa
1.
Becker muscular dystrophy: carrier detection by real-time ultrasound.
J Neurol
; 232(5): 307-9, 1985.
Artigo
Inglês
| MEDLINE | ID: mdl-3903058
2.
Atypical form of X-linked proximal pseudohypertrophic muscular dystrophy.
J Neurol
; 234(3): 163-71, 1987 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-3585425
3.
Carrier detection in X-linked Becker muscular dystrophy by muscle provocation test (MPT).
J Neurol Sci
; 62(1-3): 141-6, 1983 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-6668470
4.
Inherited deletion of subband Xp21.13 in a male with Duchenne muscular dystrophy.
J Med Genet
; 25(6): 377-82, 1988 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-3294410
5.
Epidemiological data on Werdnig-Hoffmann disease in Germany (West-Thüringen).
Hum Genet
; 91(3): 295-7, 1993 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-8478016
6.
Chronic childhood spinal muscular atrophy in Germany (West-Thüringen)--an epidemiological study.
Hum Genet
; 93(3): 344-6, 1994 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-8125489
7.
Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw.
Hum Genet
; 85(2): 211-4, 1990 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-2370051
8.
Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibships.
Hum Genet
; 76(3): 230-5, 1987 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-3596597
9.
Segregation analysis of 1885 DMD families: significant departure from the expected proportion of sporadic cases.
Hum Genet
; 84(6): 522-6, 1990 May.
Artigo
Inglês
| MEDLINE | ID: mdl-2338336
10.
Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
Biomed Biochim Acta
; 45(7): K19-27, 1986.
Artigo
Inglês
| MEDLINE | ID: mdl-2878658
11.
Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
J Med Genet
; 26(1): 1-5, 1989 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-2918522
12.
Human X chromosome markers and Duchenne muscular dystrophy.
Nucleic Acids Res
; 13(10): 3419-26, 1985 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-3859837
13.
[Quantitative computed tomographic studies of disseminated muscle changes in female carriers of Becker-Kiener muscular dystrophy]. / Quantitative computertomographische Untersuchungen zur Objektivierung disseminierter Skelettmuskelveränderungen bei Konduktorinnen der Becker-Kiener-Muskeldystrophie.
Radiol Diagn (Berl)
; 28(2): 205-16, 1987.
Artigo
Alemão
| MEDLINE | ID: mdl-3615835
14.
[Marshall syndrome. Clinico-genetic study of a family with 8 affected members]. / Marshall-Syndrom. Klinisch-genetische Untersuchung über eine Familie mit 8 Merkmalsträgern.
Kinderarztl Prax
; 56(1): 25-31, 1988 Jan.
Artigo
Alemão
| MEDLINE | ID: mdl-3361758
15.
[New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy]. / Neue Aspekte der Carrierdiagnostik und humangenetischen Beratung bei Duchenne und Becker Muskeldystrophie.
Z Arztl Fortbild (Jena)
; 82(22): 1139-42, 1988.
Artigo
Alemão
| MEDLINE | ID: mdl-3247797
16.
[The molecular principles of Duchenne and Becker muscular dystrophy and their genetic diagnosis]. / Die molekularen Grundlagen der Duchenneschen und Beckerschen Muskeldystrophie und ihre genomische Diagnostik.
Z Arztl Fortbild (Jena)
; 83(3): 117-20, 1989.
Artigo
Alemão
| MEDLINE | ID: mdl-2655303