J. Hoo

J. Hoo, H. Goedde, L. Hussein, 1977, Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie.

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Deborah L. Levy, Gregory M. Cooper, Brian L. Browning, 2010, Nature Genetics.

Chromosome 6q deletions: a report of two additional cases and a review of the literature.

J. Hoo, A. Robertson, S. B. Fowlow, 1990, American journal of medical genetics.

The Aarskog (facio‐digito‐genital) Syndrome

J. Hoo, 1979 .

Delineation of 14q32.3 deletion syndrome.

J. Hoo, C. Stein, L. L. Thomson, 1997, Journal of medical genetics.

Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin.

K. Szego, M. Chao, J. Hoo, 1995, American journal of medical genetics.

Evidence of chromosome 9 origin of the euchromatic variant band within 9qh

J. Hoo, B. Roland, P. Wong, 1993, Clinical genetics.

A new chromosome 9 variant: an extra band within the 9qh region

J. Hoo, 1992, Clinical genetics.

Supernumerary small ring chromosome

B. Zabel, J. Hoo, C. Förster, 1974, Humangenetik.

Routine application of high resolution chromosome analysis.

J. Hoo, 1986, American journal of medical genetics.

A TNNI2 mutation in a family with distal arthrogryposis type 2B.

A. Shrimpton, J. Hoo, 2006, European journal of medical genetics.

Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes

J. Rosenfeld, B. Torchia, L. Shaffer, 2011, European Journal of Human Genetics.

FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing

A. Battaglia, R. Stevenson, C. Schwartz, 2009, Genetics in Medicine.

A gene for FG syndrome maps in the Xq12-q21.31 region.

C. Romano, A. Poustka, M. Pembrey, 1997, American journal of medical genetics.

Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28).

L. Field, G. Hoganson, D. Hoar, 1992, American journal of medical genetics.

Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement

H. Pabst, R. Collins-Nakai, J. Hoo, 1986, Clinical genetics.

Confirmation of regional assignment of gene for human esterase-D to chromosome band 13q14

M. Koch, J. Hoo, B. Ziemsen, 2004, Human Genetics.

Supernumerary isochromosome 4p in ANLL-M4 myelomonocytic type is associated with favorable prognosis.

K. Szego, B. Jones, S. Gregory, 1995, Cancer genetics and cytogenetics.

β-Glucuronidase P408S, P415L mutations: evidence that both mutations combine to produce an MPS VII allele in certain Mexican patients

W. Sly, R. Vervoort, L. Valentino, 1996, Human Genetics.

Familial middle lobe bronchiectasis

J. Hoo, 1979, Clinical genetics.

In vitro effect of haloperidol, chlorpromazine, imipramine and lithium on the erythrocyte catechol-O-methyltransferase.

D. Agarwal, J. Hoo, H. Goedde, 1982, Arzneimittel-Forschung.

Alternative explanations for recurrent achondroplasia in siblings of normal parents

J. Hoo, 1984, Clinical genetics.

Partial trisomy 9q due to maternal 9/17 translocation.

S. Aftimos, J. Hoo, M. Parslow, 1980, American journal of diseases of children.

Double supernumerary isochromosome 9p in myeloproliferative syndrome.

J. Hoo, I. Samuel, S. O'Brien, 1987, Cancer genetics and cytogenetics.

The behavior of ring chromosome 13

J. Hoo, U. Obermann, H. Cramer, 2004, Humangenetik.

On the position of chromosomes in prepared mitosis figures of human fibroblasts

J. Hoo, H. Cramer, 2004, Humangenetik.

Trisomy of the short arm of chromosome 17

J. Hoo, E. Latta, 2004, Humangenetik.

Multiple, variable-sized, minute marker chromosomes.

C. Lin, J. Hoo, 1988, American journal of medical genetics.

Origin of 46,XY/46,XY,r(19) mosaicism.

D. Sobel, J. Hoo, J. Yung, 1990, American journal of medical genetics.

Combination of differential sister chromatid staining, G-banding pattern, and X-inactivation pattern

J. Hoo, M. Parslow, D. Chambers, 1979, Human Genetics.

Karyotype-phenotype analysis: 9p deletion versus 10q2 duplication.

J. Hoo, 1986, Annales de genetique.

Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.

J. Hoo, W. Fuhrmann, A. Fischer, 1982, Annales de genetique.

The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12.

J. Hoo, P. Bowen, B. Biederman, 1985, Annales de genetique.

Familial hyper‐ and hypopigmentation with age‐related pattern change

A. Shrimpton, J. Hoo, 2005, American journal of medical genetics. Part A.

A deleted extra chromosome 22 identified by DNA replication banding

J. Hoo, M. Parslow, M. Garry, 1980, Human Genetics.

A pseudoisochromosome 18q and an isodicentric chromosome 18 *

G. Hoganson, J. Hoo, A. Robertson, 1989, Clinical genetics.

The ring nature of a tiny supernumerary chromosome fragment.

M. Drummond, J. Hoo, M. Parslow, 1980, American journal of medical genetics.

New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay.

J. Hoo, F. Bacha, 2001, American journal of medical genetics.

3C (cranio-cerebello-cardiac) syndrome: a recently delineated and easily recognizable congenital malformation syndrome.

J. Hoo, A. Perszyk, M. Kreiter, 1994, American journal of medical genetics.

High resolution pattern of an inverted duplication (15)

J. Hoo, 1986, Clinical Genetics.

Succinate dehydrogenase deficiency associated with dilated cardiomyopathy and ventricular noncompaction

Zurab Davili, Sandeep Johar, Colleen Hughes, 2007, European Journal of Pediatrics.

Cytogenetics of Prader‐Willi Syndrome

J. Hoo, 1984, Clinical genetics.

Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31.

A. Shrimpton, J. Hoo, K. M. Daly, 1999, American journal of medical genetics.

Antenatal diagnosis of maple syrup urine disease

J. Hoo, E. Latta, E. Schaumlöffel, 2004, Zeitschrift für Kinderheilkunde.

DA/DAPI pattern of marker chromosome: cytogenetics of cat eye syndrome

J. Hoo, 1986, Clinical genetics.

Familial congenital funnel chest.

A. Leung, J. Hoo, 1987, American journal of medical genetics.

Interstitial 6q deletion and Prader‐Willi‐like phenotype

J. Hoo, S. Stred, C. Stein, 1996, Clinical genetics.

Familial short arm deletion of chromosome No. 15

J. Hoo, U. Hillig, S. Hansen, 2004, Humangenetik.

EVOLUTION OF X-CHROMOSOME INACTIVATION

J. Hoo, 1976, The Lancet.

The Aarskog (facio-digito-genital) syndrome.

J. Hoo, 1979, Clinical genetics.

Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters

R. Haslam, R. Lowry, J. Hoo, 1985, Clinical genetics.

Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delay

A. Shrimpton, J. Hoo, 2008, American journal of medical genetics. Part A.

Karyotype–phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit

A. Shrimpton, J. Hoo, Kimberly Jensen, 2006, American journal of medical genetics. Part A.

Pain sensitivity in schizophrenics.

D. Agarwal, J. Hoo, H. Goedde, 1979, The New England journal of medicine.

Interstitial duplication/deletion owing to unequal crossing-over in association with pericentric inversion.

J. Hoo, 1983, Journal of medical genetics.

Clinical consequence of Xp-

J. Hoo, 1979, Human Genetics.

Effect of amphetamine on brain catecholamines, brain beta-endorphin, serum prolactin, catechol-O-methyltransferase and monoamine oxidase of various organs in the rat.

D. Agarwal, A. Tjaden, J. Hoo, 1985, Arzneimittel-Forschung.