G. Wolff

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Nondirectiveness — Facts, Fiction, and Future Prospects

G. Wolff, 1999 .

Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia

M. Abramowicz, C. Bergmann, E. Holinski‐Feder, 2008, Clinical genetics.

The New Genetics: From Research into Health Care

H. Neitzel, G. Wolff, I. Nippert, 1999, Springer Berlin Heidelberg.

Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease

C. Collins, M. Hayden, O. Riess, 1992, Nature Genetics.

Nondirectiveness and genetic counseling

G. Wolff, C. Jung, 1995, Journal of Genetic Counseling.

Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.

S. Mundlos, S. Tinschert, G. Gillessen‐kaesbach, 2000, American journal of human genetics.

Neurofibromatosis 2: a clinically and genetically heterogeneous disease? Report on 10 sporadic cases

J. Gilsbach, B. Wullich, L. Mayfrank, 1990, Clinical genetics.

Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (Type VIIC) and common polymorphisms in the ADAMTS2 gene.

J. Oosterwijk, M. Thiry, A. Paepe, 2004, The Journal of investigative dermatology.

Statement on the Genetic Diagnosis of Factors that Predispose to Multifactorial Diseases, Developmental Disorders, and Drug Reactions

K. Zerres, C. Bartram, W. Henn, 2004 .

Mutations of the androgen receptor gene in patients with complete androgen insensitivity

P. Wieacker, G. Wolff, S. Jakubiczka, 1997, Human mutation.

Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations.

Priya D. Duggal, A. Beggs, G. Wolff, 1999, American journal of medical genetics.

Survival and dominant transmission of "lethal" platyspondylic dwarfism of the "West coast" types.

H. Omran, M. Uhl, G. Wolff, 2000, The Journal of pediatrics.

Rare combination of Becker muscular dystrophy and Klinefelter's syndrome in one patient

U. Ketelsen, R. Korinthenberg, G. Wolff, 1997, Brain and Development.

Aldosterone deficiency II (CMO II deficiency) is not the result of a mutation of an MspI restriction site within the CYP11B gene

B. Zieger, G. Wolff, M. Brandis, 2005, Human Genetics.

The distalmost palmar axial triradius in children with selected types of isolated congenital heart disease.

E. Hook, G. Wolff, E. Desmond, 1974, Teratology.

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)

T. Meitinger, S. Schuffenhauer, P. Lichtner, 1998, European Journal of Human Genetics.

Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome

T. Wienker, D. Kloos, P. Wieacker, 1997, Human Genetics.

Presymptomatic diagnosis in families with adenomatous polyposis using highly polymorphic dinucleotide CA repeat markers flanking the APC gene.

W. Eckert, G. Wolff, C. Jung, 1994, Journal of medical genetics.

flanking the APC gene . polymorphic dinucleotide CA repeat markers adenomatous polyposis using highly Presymptomatic diagnosis in families with

W. Eckert, G. Wolff, C. Jung, 2022 .

Location and type of mutation in the LIS1 gene do not predict phenotypic severity

J. Winkler, U. Bogdahn, G. Schuierer, 2007, Neurology.

Attitudes of at-risk persons for Huntington disease toward predictive genetic testing.

G. Wolff, W. Walter, 1992, Birth defects original article series.

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.

On the genetics of mandibular prognathism: analysis of large European noble families.

T. Wienker, G. Wolff, H. Sander, 1993, Journal of medical genetics.

Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci.

P. Wieacker, O. Hiort, G. Scherer, 2010, Human reproduction.

Clinical, cytogenetic and molecular investigations in three patients with Wolf‐Hirschhorn syndrome

G. Wolff, U. Thies, T. Schroeder-Kurth, 1992, Clinical genetics.

Assisted reproductive techniques in patients with Klinefelter syndrome: a critical review.

C. Tempfer, C. Keck, G. Wolff, 2004, Fertility and sterility.

Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations

G. Wolff, E. Back, B. Meer, 2004, Human Genetics.

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

J. Gusella, W. Koroshetz, J. Vonsattel, 1993, Nature genetics.

New mutation to Huntington's disease.

G. Deuschl, T. Wienker, C. Lücking, 1989, Journal of medical genetics.

Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfatase

H. Ropers, H. Hameister, G. Wolff, 1979, Human Genetics.

Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal life.

H. Dörr, F. Bidlingmaier, G. Wolff, 1984, The Journal of clinical endocrinology and metabolism.

Autosomal dominant and X‐linked ichthyosis in the same family. Biochemical analysis of steroid sulfatase activity

G. Wolff, E. Frenk, B. Mevorah, 1980, Clinical genetics.

Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal Xq.

T. Wienker, P. Wieacker, G. Wolff, 1987, American journal of medical genetics.

X-linked mental retardation: transmission of the trait by an apparently unaffected male.

H. Ropers, H. Hameister, G. Wolff, 1978, American journal of medical genetics.

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome.

E. Zackai, M. Muenke, D. Viskochil, 1995, Human molecular genetics.

Microdeletion 5q14.3 and anomalies of brain development

D. Saunders, A. Caliebe, I. Nagel, 2013, American journal of medical genetics. Part A.

Search for uniparental disomy 14 in balanced Robertsonian translocation carriers

T. Eggermann, C. Spaich, G. Uyanik, 1999, Clinical genetics.

Genetic Counseling Practices in Germany: A Comparison Between East German and West German Geneticists

G. Wolff, D. Wertz, I. Nippert, 1997, Journal of Genetic Counseling.

Deletion 11q23.3 without familial predisposition

I. Voiculescu, G. Wolff, E. Back, 1988, Human Genetics.

A BrdU-requiring fragile site on chromosome 12

I. Voiculescu, G. Wolff, E. Back, 1988, Human Genetics.

Prenatal Diagnosis of X-Linked Centronuclear Myopathy by Linkage Analysis

U. Ketelsen, G. Wolff, S. Liechti‐Gallati, 1993, Pediatric Research.

Genetic counseling in families with inherited balanced translocations: experience with 36 families

G. Wolff, E. Back, Sybille Arleth, 1989, Clinical genetics.

Linkage of genes for chronic granulomatous disease and Xg

G. Wolff, C. Müller, A. Jobke, 2004, Human Genetics.

Familial congenital diaphragmatic defect: Review and conclusions

G. Wolff, 2004, Human Genetics.

A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia.

J. Opitz, T. Wienker, P. Wieacker, 1985, American journal of medical genetics.

A novel ABCA12 mutation 3270delT causes harlequin ichthyosis

J. R. McMillan, M. Akiyama, H. Shimizu, 2006, The British journal of dermatology.

Familial pericentric inversion of chromosome 12

W. Schempp, I. Voiculescu, G. Barbi, 1986, Human Genetics.

Cardiovascular malformations in oculoauriculovertebral dysplasia (Goldenhar syndrome).

A. Rosenthal, G. Wolff, R. D. Greenwood, 1974, The Journal of pediatrics.

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families

I. Kennerknecht, M. Zank, E. Passarge, 1993, Human Genetics.

Novel Mutations Including Deletions of the Entire OFD1 Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability

D. Horn, K. Heimdal, D. Wieczorek, 2013, Human mutation.

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects

M. Hayden, B. Kremer, F. Squitieri, 1993, Nature genetics.

Preferential X inactivation in human placenta membranes: Is the paternal X inactive in early embryonic development of female mammals?

H. Ropers, G. Wolff, H. Hitzeroth, 1978, Human Genetics.

New mutation toHuntington's disease

T. Wienker, G. Oepen, M. Schumacher, 1989 .

Familial ring (20) chromosomal mosaicism

I. Voiculescu, G. Wolff, M. Brünger, 1989, Human Genetics.

Distribution of G6PD phenotypes in red blood cells of Southern African Negroids: Evidence for somatic selection

H. Ropers, H. Hameister, G. Wolff, 1978, Human Genetics.

Mental health and quality of life after genetic testing for Huntington disease: A long‐term effect study in Germany

J. Barth, G. Wolff, Claudia Licklederer, 2008, American journal of medical genetics. Part A.

A familial case of tricho‐rhino‐phalangeal syndrome type III with a novel missense mutation in exon 6 of the TRPS1 gene

D. Nashan, L. Bruckner-Tuderman, H. Lüdecke, 2010, Journal of the European Academy of Dermatology and Venereology : JEADV.

Instructions for use Title A novel ABCA 12 mutation 3270 delT causes harlequin ichthyosis

J. R. McMillan, H. Shimizu, I. Hausser, 2017 .

Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

T. Wienker, M. Warburg, P. Ioannou, 1992, Journal of medical genetics.

Changes in the retinal pigment epithelium close to retinal vessels in familial adenomatous polyposis

D. Schmidt, G. Wolff, C. Jung, 1994, Graefe's Archive for Clinical and Experimental Ophthalmology.

In focus. Has patient autonomy gone to far? Geneticists' views in 36 nations.

S. Aymé, G. Wolff, J. Fletcher, 2002, The American journal of bioethics : AJOB.

Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes

W. Endres, P. Klemm, G. Wolff, 1988, Journal of Inherited Metabolic Disease.

[Cerebro-costo-mandibular syndrome without cerebral involvement in a 4-year-old boy].

P. Meinecke, G. Wolff, E. Schaefer, 1987, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.

Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders

J. Winkler, S. Couillard-Després, L. Aigner, 2003, Neurology.

Isochromosome Xq in Klinefelter syndrome: report of 7 new cases.

E. Nieschlag, P. Meinecke, G. Wolff, 1996, American journal of medical genetics.

Severe mental retardation and macroorchidism without mutation in the FMR1 gene.

R. Kooy, P. Willems, E. Reyniers, 1996, American journal of medical genetics.

Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?

G. Deuschl, U. Froster-Iskenius, G. Wolff, 1991, American journal of medical genetics.

[Basic principles of genetic counseling].

G. Wolff, 1992, Diskussionsforum medizinische Ethik.

X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder

H. Ropers, U. Ketelsen, G. Wolff, 1993, Human Genetics.

Benign muscular dystrophy: risk calculation in families with consanguinity.

T. Grimm, G. Wolff, C. Müller, 1989, Journal of medical genetics.

Late manifestation of autosomal-recessive polycystic kidney disease in two sisters.

B. Wirth, K. Zerres, H. Neumann, 1988, American journal of nephrology.

Genetic Counseling: Historical, Ethical, and Practical Aspects

J. Schmidtke, H. Skirton, G. Wolff, 2001 .

Ethical issues in genetic service provision: attitudes of human geneticists in Germany.

G. Wolff, D. Wertz, I. Nippert, 1996, American journal of human genetics.

Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?

G. Wolff, E. Zimmermann, C. Jung, 1994, Journal of medical genetics.

Mutations of the androgen receptor gene in patients with complete androgen insensitivity

P. Wieacker, G. Wolff, S. Jakubiczka, 1997, Human mutation.

Mental health and quality of life after genetic testing for Huntington disease: A long‐term effect study in Germany

J. Barth, G. Wolff, Claudia Licklederer, 2008, American journal of medical genetics. Part A.