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Journal of Medical Genetics
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J Med Genet
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http://hub.abes.fr/bmj/periodical/jmedgenet/1964/volume_1
http://hub.abes.fr/bmj/periodical/jmedgenet/1965/volume_2
http://hub.abes.fr/bmj/periodical/jmedgenet/1966/volume_3
http://hub.abes.fr/bmj/periodical/jmedgenet/1967/volume_4
http://hub.abes.fr/bmj/periodical/jmedgenet/1968/volume_5
http://hub.abes.fr/bmj/periodical/jmedgenet/1969/volume_6
http://hub.abes.fr/bmj/periodical/jmedgenet/1970/volume_7
http://hub.abes.fr/bmj/periodical/jmedgenet/1971/volume_8
http://hub.abes.fr/bmj/periodical/jmedgenet/1972/volume_9
http://hub.abes.fr/bmj/periodical/jmedgenet/1973/volume_10
http://hub.abes.fr/bmj/periodical/jmedgenet/1974/volume_11
http://hub.abes.fr/bmj/periodical/jmedgenet/1975/volume_12
http://hub.abes.fr/bmj/periodical/jmedgenet/1976/volume_13
http://hub.abes.fr/bmj/periodical/jmedgenet/1977/volume_14
http://hub.abes.fr/bmj/periodical/jmedgenet/1978/volume_15
http://hub.abes.fr/bmj/periodical/jmedgenet/1979/volume_16
http://hub.abes.fr/bmj/periodical/jmedgenet/1980/volume_17
http://hub.abes.fr/bmj/periodical/jmedgenet/1981/volume_18
http://hub.abes.fr/bmj/periodical/jmedgenet/1982/volume_19
http://hub.abes.fr/bmj/periodical/jmedgenet/1983/volume_20
http://hub.abes.fr/bmj/periodical/jmedgenet/1984/volume_21
http://hub.abes.fr/bmj/periodical/jmedgenet/1985/volume_22
http://hub.abes.fr/bmj/periodical/jmedgenet/1986/volume_23
http://hub.abes.fr/bmj/periodical/jmedgenet/1987/volume_24
http://hub.abes.fr/bmj/periodical/jmedgenet/1988/volume_25
http://hub.abes.fr/bmj/periodical/jmedgenet/1989/volume_26
http://hub.abes.fr/bmj/periodical/jmedgenet/1990/volume_27
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http://hub.abes.fr/bmj/periodical/jmedgenet/1992/volume_29
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http://hub.abes.fr/bmj/periodical/jmedgenet/1994/volume_31
http://hub.abes.fr/bmj/periodical/jmedgenet/1995/volume_32
http://hub.abes.fr/bmj/periodical/jmedgenet/1996/volume_33
http://hub.abes.fr/bmj/periodical/jmedgenet/1997/volume_34
http://hub.abes.fr/bmj/periodical/jmedgenet/1998/volume_35
http://hub.abes.fr/bmj/periodical/jmedgenet/2002/volume_39
http://hub.abes.fr/bmj/periodical/jmedgenet/2003/volume_40
http://hub.abes.fr/bmj/periodical/jmedgenet/2004/volume_41
http://hub.abes.fr/bmj/periodical/jmedgenet/2005/volume_42
http://hub.abes.fr/bmj/periodical/jmedgenet/2006/volume_43
http://hub.abes.fr/bmj/periodical/jmedgenet/2007/volume_44
http://hub.abes.fr/bmj/periodical/jmedgenet/2010/volume_47
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Mongolism in Twins
Corrigenda
Congenital Hereditary Lymphoedema
Congenital anomalies due to transmission of a chromosome translocation.
Chromosome preparation from leucocyte culture. A simplified method for collecting samples by post.
13-15 trisomy mosiacism in a normal-looking 14-year-old retarded girl.
Blood group changes in leukaemia.
Apparent deletion of X chromosome in a prepuberal girl.
Family Studies on Ocular Refraction and Its Components
Haptoglobin Phenotypes Among Egyptians
Humangenetik. Ein kurzes Handbuch in fünf Bänden
Mental retardation in a child with a long B-group chromosome.
Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents.
Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients.
An Epidemiological Survey of Skin Diseases, Tattooing, and Rheumatic Diseases as Exemplified Initially by the Prevalence of Psoriasis and Tattooing
Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism.
Studies on glucose-6-phosphate dehydrogenase deficient Egyptian families.
Books and Monographs
Inhibition of the motility of gill cilia of Dreissensia by plasma of cystic fibrosis patients and their parents.
Plasma corticosteroids in healthy twin pairs.
Huntington's chorea in a Chinese family.
Books and Monographs
Anomalies of chromosome no. 3 in abortuses.
Books and Monographs
Diagnosis and Treatment of Fetal Disorders
A family with a large Y chromosome.
Familial hypertrichosis cubiti: hairy elbows syndrome.
Grundriss der Genetik
Animal models for bone-marrow transplantation.
X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data.
Advances in Twin Studies
The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry.
ABH secretor status of the fetus: a genetic marker identifiable by amniocentesis.
Genetics of the Evolutionary Process
Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.
Congenital absence of the fibula and craniosynostosis in sibs.
Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
The inheritance of dental traits in a Chinese population in the United Kingdom.
Genetic aspects of selective immunoglobulin A deficiency.
A Psychological-Psychiatric Study of Patients with Klinefelter's Syndrome, 47,XXY
Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells.
Aminoacidopathies, Immunoglobinopathies, Neuro-genetics and Neuro-ophthalmology
The Assessment of Population Affinities in Man
Trisomy 13 in Two Infants with Cyclops
Immunoglobulins.
Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria.
Extensive cytological damage caused by measles in African children
The trisomy 8 syndrome: two additional mosaic cases
Estimation of the age at onset of Huntington's disease from factors associated with the affected parent.
The Genetics of Locomotor Disorders
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