Volume 29; Issue 6

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Clinical Genetics
Volume 29; Issue 6

Clinical Genetics

Volume 29; Issue 6

1

Reciprocal effects of apolipoprotein E alleles (ε2 AND ε4) on plasma lipid levels in normolipidemic subjects

M. Eto, K. Watanabe, K. Ishii

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 554 KB

english, 1986

2

DNA polymorphisms around the apo Al gene in normal and hyperlipidaemic individuals selected for a twin study

A. M. Kessling, K. Berg, E. Mockleby, S. E. HUMPHRIES

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 379 KB

english, 1986

3

Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe : Family typing for PKU by linked Hindlll RFLP

A. Speer, H.-H. Dahl, O. Riess, G. Cobet, R. Hanke, R. G. H. Cotton, Ch. Coutelle

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 314 KB

english, 1986

4

Segregation analysis of brown oculocutaneous albinism

Richard A. King, Stephen S. Rich

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 244 KB

english, 1986

5

First trimester chorionic villi sampling and direct chromosome preparations

A. T. Tharapel, J. V. Dacus, S. A. Tharapel, J. Dempsey, G. Flinn, D. C. Shaver, D. Massouda, R. Sid Wilroy

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 501 KB

english, 1986

6

Craniofrontonasal dysplasia: clinical and genetic analysis

Christina M. Sax, David B. Flannery

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 574 KB

english, 1986

7

Xp21/autosome translocations : Case report and risk for Duchenne muscular dystrophy

Jeanette J. A. Holden, Anne Smith, Patrick M. MacLeod, Ron Masotti, Alessandra M. V. Duncan

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 482 KB

english, 1986

8

The Grant Syndrome: Persistent Wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia - an autosomal dominant trait : The Grant syndrome

J. Robert Maclean, R. Brian Lowry, Betty J. Wood

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 594 KB

english, 1986

9

A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently

D. Kumar, J. W. Clark, C. E. Blank, M. A. Patton

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 624 KB

english, 1986

10

Partial deletion of the short arm of chromosome 3

J. L. Tolmie, P. Batstone, I. Ruthven, D. H. Gilmore

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 206 KB

english, 1986

11

On the origin of extra isochromosomes

Horacio Rivera, Fernando Rivas, José MaríSa Cantú

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 138 KB

english, 1986

12

Critical segment for 9p deletion syndrome

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 149 KB

english, 1986

13

7th International Congress of Human Genetics – Satellite Workshop

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 46 KB

english, 1986

14

Third International Conference on Chorionic Villus Sampling and Early Prenatal Diagnosis

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 46 KB

english, 1986

15

ERRATUM

Journal:

Clinical Genetics

Year:

1986

File:

PDF, 16 KB

1986

16

The Human Gene Map 15 April 1986: The Morbid Anatomy of the Human Genome

Victor A. McKusick

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 2.75 MB

english, 1986

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