Anomalies chromosomiques équilibrées avec phénotype anormal = Balanced chromosomal rearrangements and abnormal phenotypeFRYNS, J.-P.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 33-36, issn 0021-7743Conference Paper

The fragile X syndrome. A study of 83 familiesFRYNS, J. P.Clinical genetics. 1984, Vol 26, Num 6, pp 497-528, issn 0009-9163Article

Gingival fibromatosis and partial duplication of the short arm of chromosome 2 dup(2)(p13→p21)FRYNS, J. P.Annales de génétique (Paris). 1996, Vol 39, Num 1, pp 54-55, issn 0003-3995Article

The cardio-facio-cutaneous (CFC) syndrome and Robertsonian 15/22 translocationFRYNS, J. P.Annales de génétique (Paris). 1992, Vol 35, Num 3, pp 186-188, issn 0003-3995Article

Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasiaFRYNS, J. P.Journal of medical genetics. 1987, Vol 24, Num 5, pp 271-274, issn 0022-2593Article

Aarskog syndrome : the changing phenotype with ageFRYNS, J. P.American journal of medical genetics. 1992, Vol 43, Num 1-2, pp 420-427, issn 0148-7299Article

Congenital scalp defects with distal limb reduction anomaliesFRYNS, J. P.Journal of medical genetics. 1987, Vol 24, Num 8, pp 493-496, issn 0022-2593Article

Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her childMOERMAN, P; FRYNS, J.-P.American journal of medical genetics. 1996, Vol 63, Num 3, pp 479-481, issn 0148-7299Article

A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasiaFRYNS, J. P; MOERMAN, P.Genetic counseling. 1995, Vol 6, Num 1, pp 65-67, issn 1015-8146Article

Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndromeSOEKARMAN, D; FRYNS, J. P.Genetic counseling. 1992, Vol 3, Num 2, pp 111-113, issn 1015-8146Article

Population cytogeneticsn of autosomal fragile sitesFRYNS, J. P; PETIT, P.Clinical genetics. 1987, Vol 31, Num 1, pp 61-63, issn 0009-9163Article

The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia: further evidence for autosomal recessive inheritanceMEINECKE, P; FRYNS, J. P.Clinical genetics. 1985, Vol 28, Num 6, pp 516-520, issn 0009-9163Article

Smith-lemli-opitz syndrome : the changing phenotype with ageDE DIE-SMULDERS, CH; FRYNS, J. P.Genetic counseling. 1992, Vol 3, Num 2, pp 77-82, issn 1015-8146Article

The fetal akinesia deformation sequence a fetopathological approachMOERMAN, P; FRYNS, J. P.Genetic counseling. 1990, Vol 1, Num 1, pp 25-33Article

Les maladies rénales polykystiques: morphologie et conseil génétique = Renal polykystic diseases. Morphology and genetic coucnilMOERMAN, P; FRYNS, J.-P.Journal de génétique humaine. 1985, Vol 33, Num 2, pp 157-165, issn 0021-7743Conference Paper

Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delaySYRROU, M; FRYNS, J.-P.Journal of medical genetics. 2001, Vol 38, Num 9, pp 621-624, issn 0022-2593Article

Corpus callosum agenesis in Coffin-Lowry syndromeSOEKARMAN, D; FRYNS, J. P.Genetic counseling. 1994, Vol 5, Num 1, pp 77-80, issn 1015-8146Conference Paper

Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features : confirmation of a distinct entity ?SOEKARMAN, D; FRYNS, J. P.Journal of medical genetics. 1993, Vol 30, Num 3, pp 245-247, issn 0022-2593Article

Miller postaxial acrofacial dysostosis the phenotypic changes with ageCHRZANOWSKA, K; FRYNS, J. P.Genetic counseling. 1993, Vol 4, Num 2, pp 131-133, issn 1015-8146Article

La tétrasomie 12p (syndrome de Pallister-Killian): un diagnostic possible avant l'âge d'un an = Tetrasomy 12p (Pallister-Killian syndrome)CHRZANOWSKA, K; FRYNS, J. P.Journal de génétique humaine. 1989, Vol 37, Num 3, pp 259-261, issn 0021-7743Conference Paper

Distal osteolysis, short stature, mental retardation, and characteristic facial appearance: delineation of an autosomal recessive subtype of essential osteolysisPETIT, P; FRYNS, J.-P.American journal of medical genetics. 1986, Vol 25, Num 3, pp 537-541, issn 0148-7299Article

Oculocerebral syndrome with hypopigmentation (cross syndrome) : the mixed pattern of hair pigmentation as an important diagnostic signDE JONG, G; FRYNS, J. P.Genetic counseling. 1991, Vol 2, Num 3, pp 151-155, issn 1015-8146Conference Paper

Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defectBUTTIENS, M; FRYNS, J. P.American journal of medical genetics. 1987, Vol 27, Num 3, pp 651-660, issn 0148-7299Article

Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX, -21, -21,+t(21;21)(p11;q11)FRYNS, J. P; KLECZKOWSKA, A.Annales de génétique (Paris). 1987, Vol 30, Num 2, pp 109-110, issn 0003-3995Article

X-linked mental retardation with marfanoid habitusFRYNS, J.-P; BUTTIENS, M.American journal of medical genetics. 1987, Vol 28, Num 2, pp 267-274, issn 0148-7299Article