1.
Supravalvular aortic stenosis : genetic and molecular dissection of a complex mutation in the elastin gene
by URBAN, Zsolt
Human genetics, 2001, Vol.109 (5), p.512-520

2.
Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay
by Urban, Z
Human genetics, 2000-06-01, Vol.106 (6), p.577-588

3.
Isolated supravalvular aortic stenosis : functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay
by URBAN, Z
Human genetics, 2000, Vol.106 (6), p.577-588

4.
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination
by FERGUSON-SMITH, M. A
Human genetics, 1990, Vol.84 (2), p.198-202

5.
Assignment of the gene encoding the human thyrotropin-releasing hormone receptor to 8q23 by fluorescence in situ hybridization
by Morrison, N
Human genetics, 1994-06, Vol.93 (6), p.716-718

6.
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1
by MORRISON, N
Human genetics, 1990, Vol.85 (1), p.130-132

7.
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31
by THERIAULT, A
Human genetics, 1989, Vol.83 (3), p.289-291

8.
Regional chromosomal assignment of genes encoding the α and β subunits of human complement protein C8 to 1p32
by THERIAULT, A
Human genetics, 1992, Vol.88 (6), p.703-704

9.

10.
Regional chromosomal assignment of the human platelet phosphofructokinase gene to 10p15
by MORRISON, N
Human genetics, 1992, Vol.89 (1), p.105-106

11.
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in down syndrome
by GALT, J
Human genetics, 1989, Vol.81 (2), p.113-119

12.
Assignment of the gene encoding the human gonadotropin-releasing hormone receptor to 4q13.2-13.3 by fluorescence in situ hybridization
by MORRISON, N
Human genetics, 1994, Vol.93 (6), p.714-715

13.
Regional chromosomal assignment of human 3-beta-hydroxy-5-ene steroid dehydrogenase to 1p13.1 by non-isotopic in situ hybridisation
by MORRISON, N
Human genetics, 1991, Vol.87 (2), p.223-225

14.
Chromosomal assignment of a glutamic acid transfer RNA (tRNAGlu) gene to 1p36
by BOYD, E
Human genetics, 1989, Vol.81 (2), p.153-156

15.
Regional assignment of the human C1-inhibitor gene to 11q11-Q13.1
by THERIAULT, A
Human genetics, 1990, Vol.84 (5), p.477-479

16.
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?
by Tolmie, J L
Human genetics, 1988-10, Vol.80 (2), p.197-200

17.
Assignment of the gene encoding the human thyrotrophin-releasing hormone receptor to 8q23 by fluorescence in situ hybridization
by MORRISON, N
Human genetics, 1994, Vol.93 (6), p.716-718

18.
Human ferritin H and L sequences lie on ten different chromosomes
by MCGILL, J. R
Human genetics, 1987, Vol.76 (1), p.66-72

19.
Optimising human chromosome separation for the production of chromosome-specific DNA libraries by flow sorting
by HARRIS, P
Human genetics, 1985, Vol.70 (1), p.59-65

20.
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry
by WILCOX, D. E
Human genetics, 1986, Vol.73 (2), p.175-180
