A SYNDROME OF HYPOGONADISM, ALOPECIA, DIABETES MELLITUS, MENTAL RETARDATION, DEAFNESS, AND ECG ABNORMALITIESWOODHOUSE NJY; SAKATI NA.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 3; PP. 216-219; BIBL. 9 REF.Article

THE SYNDROME OF YUNIS AND VARON-REPORT OF A FURTHER CASEHUGHES HE; PARTINGTON MW.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 3; PP. 539-544; BIBL. 1 REF.Article

SYNDROME OF ICHTHYOSIS CONGENITA, NEUROSENSORY DEAFNESS, OLIGOPHRENIA, DENTAL APLASIA, BRACHYDACTYLY, CLINODACTYLY, ACCESSORY CERVICAL RIBS AND CARCINOMA OF THE THYROIDRUZICKA T; GOERZ G; ANTON LAMPRECHT I et al.1981; DERMATOLOGICA; ISSN 0011-9075; CHE; DA. 1981; VOL. 162; NO 2; PP. 124-136; BIBL. 32 REF.Article

Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeCHEN, H; IMMKEN, L; GILBERT, E. F et al.American journal of medical genetics. 1984, Vol 17, Num 4, pp 809-826, issn 0148-7299Article

DOMINANTLY INHERITED SYNDROME OF MICROCEPHALY AND CLEFT PALATEHALAL F.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 135-140; BIBL. 2 P.Article

UNILATERAL PARTIAL TIBIA DEFECT WITH PREAXIAL POLYDACTYLY, GENERAL MICROMELIA, AND TRIGONOMACROCEPHALY WITH A NOTE ON "DEVELOPMENTAL RESISTANCE"WIEDEMANN HR; OPITZ JM.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 3; PP. 467-471; BIBL. 12 REF.Article

KONGENITALE FEHLBILDUNGEN IM BEREICH DES AUGES UND DEREN BEDEUTUNG FUER DIE DIAGNOSTIK UEBERGEORDNETER KRANKHEITSBILDER UND DIE GENETISCHE BERATUNG = MALFORMATIONS CONGENITALES OCULAIRES ET LEUR IMPORTANCE POUR LE DIAGNOSTIC DES SYNDROMES GENERAUX ET LE CONSEIL GENETIQUEBURCK U; BROENNEKE J; HELD KR et al.1983; KLINISCHE MONATSBLAETTER FUER AUGENHEILKUNDE; ISSN 0023-2165; DEU; DA. 1983; VOL. 183; NO 1; PP. 22-27; ABS. ENG; BIBL. 6 REF.Article

OCULO-CEREBRO RENAL SYNDROME: FAILURE TO DEMONSTRATE SPECIFIC NEUROPATHOLOGICAL ABNORMALITIES IN FOUR CASESBANERGEE AK; ALLEN IV; MCKEE P et al.1982; IR. J. MED. SCI.; ISSN 0021-1265; IRL; DA. 1982; VOL. 151; NO 2; PP. 42-45; BIBL. 11 REF.Article

OTOLOGICAL ASPECTS OF THE EARPIT-DEAFNESS SYNDROMECREMERS CWRJ; THIJSSEN HOM; FISCHER AJEM et al.1981; ORL, J. OTO-RHINO-LARYNGOL. RELAT. SPEC.; CHE; DA. 1981; VOL. 43; NO 4; PP. 223-239; BIBL. 2 P.Article

ENCEPHALOCELE (CEREBELLOCELE) IN THE GOLDENHAR-GORHIN SYNDROMEALEKSIC S; BUDZILOVICH G; GRECO MA et al.1983; EUROPEAN JOURNAL OF PEDIATRICS; ISSN 0340-6199; DEU; DA. 1983; VOL. 140; NO 2; PP. 137-138; BIBL. 8 REF.Article

GOLDENHAR ASSOCIATION AND CRANIAL DEFECTSPAULI RM; JUNG JH; MCPHERSON EW et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 177-179; BIBL. 2 REF.Article

SYNDROME DE GOLDENHAR: DYSPLASIE OCULO-AURICULO-VERTEBRALE. DEUX NOUVELLES OBSERVATIONS PEDIATRIQUESPRIGENT F; RAMEL F; VALLETEAU DE MOULLIAC J et al.1983; ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE; ISSN 0151-9638; FRA; DA. 1983; VOL. 110; NO 4; PP. 345-349; ABS. ENG; BIBL. 15 REF.Article

A SYNDROME OF CONGENITAL THROMBOCYTOPENIA WITH MULTIPLE MALFORMATIONS AND NEUROLOGIC DYSFUNCTIONGARDNER RJM; MORRISON PS; ABBOTT GD et al.1983; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1983; VOL. 102; NO 4; PP. 600-602; BIBL. 14 REF.Article

CONSIDERATIONS SUR LES LIMITES DU SYNDROME DE STAUFFER: A PROPOS DE DEUX CAS CLINIQUESGIANNOTTI P; ARAGONA F; GALLIA PL et al.1982; ACTA UROL. BELG.; ISSN 0001-7183; BEL; DA. 1982; VOL. 50; NO 1; PP. 33-38; ABS. ENG; BIBL. 21 REF.Article

CEREBRAL GIGANTISM ASSOCIATED WITH JAW CYST BASAL CELL NAEVOID SYNDROME IN TWO FAMILIESCRAMER H; NIEDERDELLMANN H.1983; ARCHIV FUER PSYCHIATRIE UND NERVENKRANKENHEITEN; ISSN 0003-9373; DEU; DA. 1983; VOL. 233; NO 2; PP. 111-124; ABS. GER; BIBL. 21 REF.Article

KANTAGENER'S SYNDROME AND ABNORMAL CILIA, COPENHAGEN, MAY 27-28, 1982MYGIND N ED; NEILSEN MH ED; PEDERSEN M ED et al.1983; EUROPEAN JOURNAL OF RESPIRATORY DISEASES. SUPPLEMENT; ISSN 0106-4347; DNK; DA. 1983; VOL. 64; NO 127; 171 P.; BIBL. DISSEM.Conference Paper

DUBOWITZ-SYNDROM UND AKUTE LYMPHATISCHE LEUKAEMIE = SYNDROME DE DUBOWITZ ET LEUCEMIE LYMPHOBLASTIQUEGROEBE H.1983; MONATSSCHRIFT FUER KINDERHEILKUNDE; ISSN 0026-9298; DEU; DA. 1983; VOL. 131; NO 7; PP. 467-468; ABS. ENG; BIBL. 13 REF.Article

GLYCOSAMINOGLYCAN SYNTHESIS BY CULTURED SKIN FIBROBLASTS FROM A PATIENT WITH LOWE'S SYNDROMEFUKUI S; YOSHIDA H; TANAKA T et al.1981; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1981; VOL. 256; NO 20; PP. 10313-10318; BIBL. 14 REF.Article

STAPHYLOCIDAL DEFECT OF POLYMORPHONUCLEAR LEUKOCYTES IN A PATIENT WITH LEPRECHAUNISMSACCHI F; MAGGIORE G; BIANCHI E et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 137; NO 1; PP. 89-90; BIBL. 10 REF.Article

A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosisCLAYTON-SMITH, J; DONNAI, D.Journal of medical genetics. 1989, Vol 26, Num 5, pp 339-342, issn 0022-2593, 4 p.Article

GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible new recessively inherited MCA/MR syndromeVERLOES, A; DELFORTRIE, J; LAMBOTTE, C et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 15-18, issn 0148-7299, 4 p.Article

A combinatorial method for grouping cases with multiple malformationsWINTER, R. M; CLARK, R. D; ASHLEY, K et al.Journal of medical genetics. 1988, Vol 25, Num 2, pp 118-121, issn 0022-2593Article

Lymphedema in Noonan's syndromeWHITE, S. W.International journal of dermatology. 1984, Vol 23, Num 10, pp 656-657, issn 0011-9059Article

Carpenter syndrome: natural history and clinical spectrumROBINSON, L. K; JAMES, H. E; MUBARAK, S. J et al.American journal of medical genetics. 1985, Vol 20, Num 3, pp 461-469, issn 0148-7299Article

Sixty-four patients with Brachmann-de Lange syndrome: a surveyHAWLEY, P. P; JACKSON, L. G; KURNIT, D. M et al.American journal of medical genetics. 1985, Vol 20, Num 3, pp 453-459, issn 0148-7299Article